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Smith's recognizable patterns of human malformation

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Jones, Kenneth Lyons. Philadelphia, PA: Elsevier Saunders , 2006. 6th ed.

Material Type: Book

Call Number: REF AB 20 JON 2006

Availability: 2 copies, 2 available

Table of Contents; 1. Recognizable Patterns of Malformation; A. Chromosomal Abnormality Syndromes; Down Syndrome--Trisomy 18 Syndrome --Trisomy 13 Syndrome --Trisomy 8 Syndrome Trisomy 9 --Mosaic Syndrome --Triploidy Syndrome and Diploid/Triploid Mixoploidy Syndrome --Deletion 3p Syndrome Duplicati…

Author: Jones, Kenneth Lyons

Edition: 6th ed.

Place of Publication: Philadelphia, PA

Publisher: Elsevier Saunders

Publication Date: 2006

Physical Description: Hardcover: 954 p.

Subject: Medical Encyclopedias; Birth Defects. Congenital Abnormalities; UBC MD Undergrad

Abstract: Table of Contents; 1. Recognizable Patterns of Malformation; A. Chromosomal Abnormality Syndromes; Down Syndrome--Trisomy 18 Syndrome --Trisomy 13 Syndrome --Trisomy 8 Syndrome Trisomy 9 --Mosaic Syndrome --Triploidy Syndrome and Diploid/Triploid Mixoploidy Syndrome --Deletion 3p Syndrome Duplication 3q Syndrome Deletion 4p Syndrome --Deletion 4q Syndrome --Deletion 5p Syndrome --Deletion 9p Syndrome --Duplication 10q Syndrome --Aniridia–Wilms Tumor Association --Deletion 11q Syndrome --Deletion 13q Syndrome --Duplication 15q Syndrome-- Deletion 18p Syndrome-- Deletion 18q Syndrome --Cat-Eye Syndrome --XYY Syndrome --XXY Syndrome, Klinefelter Syndrome XXXY and XXXXY Syndromes XXX and --XXXX Syndromes XXXXX Syndrome --45X Syndrome; --; B. Very Small Stature, Not Skeletal Dysplasia; Brachmann–De Lange Syndrome --Rubinstein-Taybi Syndrome --Russell-Silver Syndrome --Short Syndrome --3-M Syndrome --Mulibrey Nanism Syndrome --Dubowitz Syndrome --Bloom Syndrome --Johanson-Blizzard Syndrome --Seckel Syndrome Hallermann-Streiff Syndrome; C. Moderate Short Stature, Facial, +/- Genital; Smith-Lemli-Opitz Syndrome --Kabuki Syndrome --Williams Syndrome Noonan Syndrome --Costello Syndrome Cardio-Facio-Cutaneous (CFC)Syndrome --Aarskog Syndrome --Robinow Syndrome --Opitz G/BBB Syndrome --Floating-Harbor Syndrome; D. Senile-Like Appearance; Progeria Syndrome Wiedemann-Rautenstrauch Syndrome --Werner Syndrome --Cockayne Syndrome Rothmund-Thomson Syndrome; E. Early Overgrowth with Associated Defects; Fragile X Syndrome --Sotos Syndrome --Weaver Syndrome --Marshall-Smith Syndrome --Beckwith-Wiedemann Syndrome --Simpson-Golabi-Behmel Syndrome; F. Unusual Brain and/or Neuromuscular Findings With Associated Defects; Amyoplasia Congenita Disruptive Sequence Distal Arthrogryposis Syndrome, Type 1 -- Pena-Shokeir Phenotype --Cerebro-Oculo-Facio-Skeletal (COFS) Syndrome --Lethal Multiple Pterygium Syndrome --Neu-Laxova Syndrome --Restrictive Dermopathy Meckel-Gruber Syndrome --Pallister-Hall Syndrome --X-Linked Hydrocephalus Spectrum Hydrolethalus Syndrome --Walker-Warburg Syndrome Miller-Dieker Syndrome Smith-Magenis Syndrome Ataxia-Telangiectasia Syndrome Menkes Syndrome 22q13 Deletion Syndrome --Angelman Syndrome Prader-Willi Syndrome --Cohen Syndrome --Killian/Teschler-Nicola Syndrome 1p36 --Deletion Syndrome --Fryns Syndrome Zellweger Syndrome --Freeman-Sheldon Syndrome --Myotonic Dystrophy Syndrome --Schwartz-Jampel Syndrome --Marden-Walker Syndrome --Schinzel-Giedion Syndrome --Acrocallosal Syndrome --3C Syndrome --Hecht Syndrome; G. Facial Defects As Major Feature; Moebius Sequence --Blepharophimosis-Ptosis-Epicanthus Inversus Synrome --Robin Sequence --Cleft Lip Sequence --Van Der Woude Syndrome Frontonasal Dysplasia Sequence Fraser Syndrome --Melnick-Fraser Syndrome --Branchio-Oculo-Facial Syndrome --Charge Syndrome --Waardenburg Syndrome, Types I and II-- Treacher Collins Syndrome --Marshall Syndrome --Cervico-Oculo-Acoustic Syndrome; H. Facial-Limb Defects as Major Feature; Miller Syndrome --Nager Syndrome --Townes-Brocks Syndrome --Oral-Facial-Digital Syndrome --Mohr Syndrome --Deletion 22q11.2 --Oculodentodigital Syndrome --Lenz Microphthalmia Syndrome --Oto-Palato-Digital Syndrome, Type I --Oto-Palato-Digital Syndrome, Type II --Coffin-Lowry Syndrome X-Linked ?--Thalassemia/Mental Retardation (ATR-X) Syndrome --FG Syndrome Stickler Syndrome --Catel-Manzke Syndrome --Langer-Giedion Syndrome --Tricho-Rhino-Phalangeal Syndrome, Type I --Ectrodactyly–Ectodermal Dysplasia–Clefting Syndrome --Hay-Wells Syndrome Of Ectodermal Dysplasia --Roberts Syndrome; I. Limb Defect as Major Feature; Grebe Syndrome --Poland Sequence --Ulnar-Mammary Syndrome --Popliteal Pterygium Syndrome --Escobar Syndrome --Child Syndrome --Femoral Hypoplasia-Unusual Facies Syndrome --Tibial Aplasia-Ectrodactyly Syndrome --Adams-Oliver Syndrome --Holt-Oram Syndrome --Levy-Hollister Syndrome --Fanconi Pancytopenia Syndrome --Radial Aplasia–Thrombocytopenia Syndrome --Aase Syndrome; J. Osteochondrodysplasias; Achondrogenesis, Types IA And IB --Type II Achondrogenesis-Hypochondrogenesis --Fibrochondrogenesis Atelosteogenesis, Type I --Short Rib–Polydactyly Syndrome, Type I (Saldino- Noonan Type)-- Short Rib–Polydactyly Syndrome, Type II (Majewski Type) --Thanatophoric Dysplasia --Jeune Thoracic Dystrophy --Campomelic Dysplasia Achondroplasia Hypochondroplasia --Pseudoachondroplasia Acromesomelic-- Dysplasia Spondyloepiphyseal --Dysplasia Congenita Kniest Dysplasia-- Dyggve-Melchior-Clausen Syndrome --Spondylometaphyseal Dysplasia, Kozlowski Type Metatropic Dysplasia --Geleophysic Dysplasia --Chondroectodermal Dysplasia --Diastrophic Dysplasia X-Linked --Recessive Spondyloepiphyseal --Dysplasia Tarda Multiple Epiphyseal-- Dysplasia Metaphyseal Dysplasia, --Schmid Type Metaphyseal Dysplasia, --Mckusick Type Metaphyseal Dysplasia,-- Jansen Type Shwachman-Diamond Syndrome Chondrodysplasia Punctata, --X-Linked Dominant Type Autosomal Recessive --Chondrodysplasia Punctata Hypophosphatasia --Hajdu-Cheney Syndrome --Craniometaphyseal Dysplasia --Frontometaphyseal Dysplasia; K. Osteochondrodysplasia with Osteopetrosis; Osteopetrosis: Autosomal Recessive—Lethal --Sclerosteosis --Lenz-Majewski --Hyperostosis Syndrome Pyknodysostosis --Cleidocranial Dysostosis --Yunis-Varon Syndrome; L. Craniosynostosis Syndromes; Saethre-Chotzen Syndrome --Pfeiffer Syndrome --Apert Syndrome --Crouzon Syndrome FGFR3- Associated Coronal Synostosis Syndrome --Craniofrontonasal Dysplasia --Carpenter Syndrome --Greig Cephalopolysyndactyly Syndrome --Antley-Bixler Syndrome Baller-Gerold Syndrome; M. Other Skeletal Dysplasias; Multiple Synostosis Syndrome --Spondylocarpotarsal Synostosis Syndrome --Larsen Syndrome --Multiple Exostoses Syndrome --Nail-Patella Syndrome --Meier-Gorlin Syndrome --Leri-Weill Dyschondrosteosis --Langer Mesomelic Dysplasia --Acrodysostosis --Albright Hereditary Osteodystrophy; N. Storage Disorders; Generalized Gangliosidosis Syndrome, Type I (Severe Infantile Type) --Leroy I-Cell Syndrome --Pseudo-Hurler Polydystrophy Syndrome --Hurler Syndrome --Scheie Syndrome --Hurler-Scheie Syndrome --Hunter Syndrome --Sanfilippo Syndrome --Morquio Syndrome --Maroteaux-Lamy Mucopolysaccharidosis Syndrome (Mild, Moderate, and Severe Types) Mucopolysaccharidosis VII1. *-*--; O. Connective Tissue Disorders; Marfan Syndrome-- Beals Syndrome --Shprintzen-Goldberg Syndrome --Ehlers-Danlos Syndrome --Osteogenesis Imperfecta Syndrome, Type I --Osteogenesis Imperfecta Syndrome, Type II --Fibrodysplasia Ossificans Progressiva Syndrome; P. Hamartoses; Sturge-Weber Sequence --Neurocutaneous Melanosis Sequence --Linear Sebaceous Nevus Sequence --Incontinentia Pigmenti Syndrome --Hypomelanosis of Ito Tuberous Sclerosis Syndrome --Neurofibromatosis Syndrome --McCune-Albright Syndrome-- Klippel-Trenaunay Syndrome --Proteus Syndrome --Encephalocraniocutaneous Lipomatosis Maffucci Syndrome-- Peutz-Jeghers Syndrome --Bannayan-Riley-Ruvalcaba Syndrome --Hereditary Hemorragic Telangiectasia-- Multiple Endocrine Neoplasia, Type 2b --Gorlin Syndrome --Multiple Lentigines Syndrome --Goltz Syndrome Microphthalmia–Linear --Skin Defects Syndrome; Q. Ectodermal Dysplasias; Hypohidrotic Ectodermal Dysplasia Syndrome --Rapp-Hodgkin Ectodermal Dysplasia Syndrome --Tricho-Dento-Osseous Syndrome --Clouston Syndrome --GAPO Syndrome --Pachyonychia Congenita Syndrome --Xeroderma Pigmentosa Syndrome --Senter-Kid Syndrome; R. Enviornmental Agents; Fetal Alcohol Syndrome --Fetal Hydantoin Syndrome --Fetal Valproate Syndrome --Fetal Warfarin Syndrome --Fetal Aminopterin/Methotrexate --Syndrome Retinoic Acid Embryopathy --Fetal Varicella Syndrome --Hyperthermia-Induced Spectrum of Defects; S. Miscellaneous Syndromes; Coffin-Siris Syndrome --Börjeson-Forssman-Lehmann Syndrome --Alagille Syndrome-- Melnick-Needles Syndrome --Bardet-Biedl Syndrome --Mckusick-Kaufman Syndrome --Rieger Syndrome --Peters' Plus Syndrome --Toriello-Carey Syndrome --Mowat-Wilson Syndrome --Cerebro-Costo-Mandibular Syndrome --Jarcho-Levin Syndrome --Mandibuloacral Dysplasia --Berardinelli Lipodystrophy Syndrome-- Distichiasis-Lymphedema Syndrome; T. Miscellaneous Sequences; Laterality Sequences --Holoprosencephaly Sequence --Meningomyelocele, Anencephaly, Iniencephaly Sequences Occult Spinal Dysraphism Sequence Septo-Optic --Dysplasia Sequence Athyrotic --Hypothyroidism Sequence --DiGeorge Sequence --Klippel-Feil Sequence Early Urethral Obstruction Sequence-- Exstrophy of Bladder Sequence --Exstrophy of Cloaca Sequence --Urorectal Septum Malformation --Sequence Oligohydramnios Sequence --Sirenomelia Sequence-- Caudal Dysplasia Sequence-- Amnion Rupture Sequence --Limb–Body Wall Complex; U. Spectra Of Defects; Oculo-Auriculo-Vertebral Spectrum --Oromandibular-Limb Hypogenesis Spectrum --Congenital Microgastria-Limb Reduction Complex --Sternal Malformation-Vascular Dysplasia --Spectrum Monozygotic (MZ) Twinning And Structural Defects - General; V. Miscellaneous Associations; VATER Association MURCS Association; 2. Approaches to Categorical Problems of Growth Deficiency, Mental Deficiency, Arthrogryposis, Ambiguous External Genitalia 3. Morphogenesis and Dysmorphogenesis 4. Genetics, Genetic Counseling, and Prevention 5. Minor Anomalies as Clues to More Serious Problems and Toward the Recognition of Malformation Syndromes 6. Normal Standards

Notes: New to this Edition; 1,000 new full-color figures and photographs.; Includes updates for every disorder, with extensive new information on the molecular basis of malformations as well as new clinical information for many disorders.; Covers 16 additional commonly seen disorders, including Deletion 1p36 syndrome * Deleletion 22q13 syndrome * Meier-Gorlin Syndrome * Short Syndrome * 3-C Syndrome * GAPO Syndrome * Lenz Microphthalmia Syndrome * Muenke Craniosynostosis * Torriello-Carey Syndrome * Mandibulo-Acral Syndrome * Mowat-Wilson Syndrome * Ulnar-Mammary Syndrome * Kaufman-McKusick Syndrome * Smith-Maginess Syndrome * Wiedeman-Rautenstrauch Syndrome * and Shprintzen-Golberg Syndrome.; Presents a wealth of new Growth Charts, plus complete revisions to existing Growth Charts.

ISBN: 978-0-7216-0615-6

Language: English

Material Type: Book

Call Number: REF AB 20 JON 2006

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Learning as a way of being: Strategies for survival in a world of permanent white water

https://cwslc.andornot.com/en/permalink/catalog109460

Vaill, Peter. San Francisco, CA: Jossey-Bass , 1996.

Material Type: Book

Call Number: REF AA 75 VAI 1996

Availability: 2 copies, 2 available

Offers a critique of the roots of management education and argues that institutions of higher learning must teach managers how to integrate the discipline of learning into their very being.

Author: Vaill, Peter

Place of Publication: San Francisco, CA

Publisher: Jossey-Bass

Publication Date: 1996

Physical Description: Hardcover;218 p.

Series: Business Management Series

Subject: Administration; Leadership/Coaching

Abstract: Offers a critique of the roots of management education and argues that institutions of higher learning must teach managers how to integrate the discipline of learning into their very being.

ISBN: 0787902462

Language: English

Material Type: Book

Call Number: REF AA 75 VAI 1996

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Now, discover your strengths

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Buckingham, Marcus, Clifton, Donald. New York, NY: The Free Press , 2001.

Material Type: Book

Call Number: REF AA 500 BUC 2001

Availability: 3 copies, 3 available

This book stresses the importance of focusing on "strengths," whether a job seeker, employee, or manager. Explains why focusing on weaknesses, and thus trying to repair flaws, can be self-defeating for individuals and organizations. Includes a questionnaire for discovering one's top-five inborn tal…

Author: Buckingham, Marcus; Clifton, Donald

Place of Publication: New York, NY

Publisher: The Free Press

Publication Date: 2001

Physical Description: Paperback; 260 p.

Subject: Administration; Work Behaviour; Job Satisfaction

Abstract: This book stresses the importance of focusing on "strengths," whether a job seeker, employee, or manager. Explains why focusing on weaknesses, and thus trying to repair flaws, can be self-defeating for individuals and organizations. Includes a questionnaire for discovering one's top-five inborn talents.

ISBN: 0743201140

Language: English

Material Type: Book

Call Number: REF AA 500 BUC 2001

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Quiet leadership: Help people think better -- don't tell them what to do: Six steps to transforming performance at work

https://cwslc.andornot.com/en/permalink/catalog109531

Rock, David. New York, NY: Collins , 2006. 1st edition.

Material Type: Book

Call Number: REF AA 75 ROC 2006

Availability: 37 copies, 34 available

Discusses the key principles of leadership that promote effective thinking and positive change, offering a simple five-step program to help managers bring out the best in their colleagues and create high-performance teams.

Author: Rock, David

Edition: 1st edition

Place of Publication: New York, NY

Publisher: Collins

Publication Date: 2006

Physical Description: Hardcover: 262 p.; Softcover: 262 p.

Subject: Administration; Leadership/Coaching

Abstract: Discusses the key principles of leadership that promote effective thinking and positive change, offering a simple five-step program to help managers bring out the best in their colleagues and create high-performance teams.

Notes: RESTRICTED TO PHSA LEADERSHIP COACHING PARTICIPANTS ONLY.; March 24/14 - Item 011999 marked as missing; March 24/14 - Item 012190 marked as missing

ISBN: 0060835907

Language: English

Material Type: Book

Call Number: REF AA 75 ROC 2006

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Creating a culture of collaboration

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Schuman, Sandy (Ed.). San Francisco, CA: Jossey-Bass , 2006.

Website: http://www.josseybass.com/WileyCDA/WileyTitle/productCd-0787981168.html

Material Type: Book

Call Number: REF AA 500 SCH 2006

Availability: 1 copy, 1 available

Collaboration is often viewed as a one-time or project-oriented activity. An increasing challenge is to help organizations incorporate collaborative values and practices in their everyday ways of working. In Creating a Culture of Collaboration, an international group of practitioners and researcher…

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Website: http://www.josseybass.com/WileyCDA/WileyTitle/productCd-0787981168.html

Author: Schuman, Sandy (Ed.)

Corporate Author: International Association of Facilitators

Place of Publication: San Francisco, CA

Publisher: Jossey-Bass

Publication Date: 2006

Physical Description: Hardcover, 498 p.

Series: Business & Management Series

Subject: Administration

Abstract: Collaboration is often viewed as a one-time or project-oriented activity. An increasing challenge is to help organizations incorporate collaborative values and practices in their everyday ways of working. In Creating a Culture of Collaboration, an international group of practitioners and researchers–from Australia, Belgium, Canada, Chile, New Zealand, Northern Ireland, United Kingdom, and the United States–provide proven approaches to creating a culture of collaboration within and among groups, organizations, communities, and societies.

ISBN: 0-7879-8116-8

Language: English

Material Type: Book

Call Number: REF AA 500 SCH 2006

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http://www.josseybass.com/WileyCDA/WileyTitle/productCd-0787981168.html

The handbook of leadership development evaluation

https://cwslc.andornot.com/en/permalink/catalog109809

Hannum, Kelly (Editor), Martineau, Jennifer W. (Editor), Reinelt, Claire (Editor). San Francisco, CA: Jossey-Bass , 2007. 1st ed.

Material Type: Book

Call Number: REF AA 500 HAN 2007

Availability: 1 copy, 1 available

With the increase in the number of organizational leadership development programs, there is a pressing need for evaluation to answer important questions, improve practice, and inform decisions. The Handbook is a comprehensive resource filled with examples, tools, and the most innovative models and …

Author: Hannum, Kelly (Editor); Martineau, Jennifer W. (Editor); Reinelt, Claire (Editor)

Edition: 1st ed.

Place of Publication: San Francisco, CA

Publisher: Jossey-Bass

Publication Date: 2007

Physical Description: Paperback, 632 p.

Subject: Administration; Program Evaluation

Abstract: With the increase in the number of organizational leadership development programs, there is a pressing need for evaluation to answer important questions, improve practice, and inform decisions. The Handbook is a comprehensive resource filled with examples, tools, and the most innovative models and approaches designed to evaluate leadership development in a variety of settings. It will help you answer the most common questions about leadership development efforts, including:; What difference does leadership development make?; What development and support strategies work best to enhance leadership?; Is the time and money spent on leadership development worthwhile?; What outcomes can be expected from leadership development?; How can leadership development efforts be sustained?

Notes: For PHSA Staff only

ISBN: 978-0-7879-8217-1

Language: English

Material Type: Book

Call Number: REF AA 500 HAN 2007

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Encyclopedia of genetic disorders and birth defects

https://cwslc.andornot.com/en/permalink/catalog110555

Wynbrandt, James., Ludman, Mark D. New York, NY: Facts On File (Infobase) , 2008. 3rd ed.

Material Type: Book

Call Number: REF GI 20 WYN 2008

Availability: 1 copy, 1 available

Topics cover everything from the most basic genetic concepts to the latest screening and diagnostic techniques. Coverage includes:; autism, cancer, chromosomal abnormalities, ethics, genetic counseling, heart defects, muscular dystrophy, neural tube defects, phenylketonuria, spina bifida, and much …

Author: Wynbrandt, James.; Ludman, Mark D.

Edition: 3rd ed.

Place of Publication: New York, NY

Publisher: Facts On File (Infobase)

Publication Date: 2008

Physical Description: Hardcover, 682 p.

Subject: Genetics/Genetic Disorders-Encyclopedias; Genetic Disorders; Birth Defects. Congenital Abnormalities; Children's Health-Encyclopedias; UBC MD Undergrad

Abstract: Topics cover everything from the most basic genetic concepts to the latest screening and diagnostic techniques. Coverage includes:; autism, cancer, chromosomal abnormalities, ethics, genetic counseling, heart defects, muscular dystrophy, neural tube defects, phenylketonuria, spina bifida, and much more.

ISBN: 9780816063963

Language: English

Material Type: Book

Call Number: REF GI 20 WYN 2008

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Patients come second: Leading change by changing the way you lead

https://cwslc.andornot.com/en/permalink/catalog113864

Spiegelman, Paul, Berrett, Britt. New York, NY: An Inc. Original , 2013.

Material Type: Book

Call Number: REF JB 200 SPI 2013

Availability: 4 copies, 4 available

Patients Come Second shakes up the traditional healthcare model, arguing that in order to care for and retain patients, leaders must first create exceptional teams and find ways to engage nurses, administrative staff, physicians, supervisors, and even housekeeping staff and switchboard operators. B…

Author: Spiegelman, Paul; Berrett, Britt

Place of Publication: New York, NY

Publisher: An Inc. Original

Publication Date: 2013

Physical Description: Hardcover, 208 p.

Subject: Change Management; Administration; Hospitals; Leadership/Coaching

Abstract: Patients Come Second shakes up the traditional healthcare model, arguing that in order to care for and retain patients, leaders must first create exceptional teams and find ways to engage nurses, administrative staff, physicians, supervisors, and even housekeeping staff and switchboard operators. By connecting employees' work with a higher purpose and equipping them with the tools to become leaders themselves, patient care can be dramatically transformed. And with continuing healthcare changes on the horizon and ever-rising pressure to acquire and keep patients, doing so now is more important than ever.

ISBN: 9780988842809

Language: English

Material Type: Book

Call Number: REF JB 200 SPI 2013

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A guide to the project management body of knowledge: PMBOK (R) Guide

https://cwslc.andornot.com/en/permalink/catalog113878

Project Management Institute. Newtown Square, PA: Project Management Institute , 2013. 5th ed.

Material Type: Book

Call Number: REF AA 74 PMI 2013

Availability: 1 copy, 1 available

The PMBOK Guide - Fifth edition reflects the collaboration and knowledge of working project managers and provides the fundamentals of project management as they apply to a wide range of projects. This internationally recognized standard gives project managers the essential tools to practice project…

Corporate Author: Project Management Institute

Edition: 5th ed.

Place of Publication: Newtown Square, PA

Publisher: Project Management Institute

Publication Date: 2013

Physical Description: Softcover, 589 p.

Subject: Administration

Abstract: The PMBOK Guide - Fifth edition reflects the collaboration and knowledge of working project managers and provides the fundamentals of project management as they apply to a wide range of projects. This internationally recognized standard gives project managers the essential tools to practice project management and deliver organizational results.

ISBN: 9781935589679

Language: English

Material Type: Book

Call Number: REF AA 74 PMI 2013

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Success on the wards: 250 rules for clerkship success

https://cwslc.andornot.com/en/permalink/catalog114586

Desai, Samir P., Katta, Rajani. Houston, TX: MD2B , 2011.

Material Type: Book

Call Number: REF AA 500 DES 2011

Availability: 1 copy, 1 available

The book begins as a how-to guide, with clerkship-specific templates, such as op notes and admission orders, along with sample notes and guides for every aspect of core clerkships (internal medicine, surgery, pediatrics, obstetrics/gynecology, psychiatry, family medicine). The book reviews proven s…

Author: Desai, Samir P.; Katta, Rajani

Place of Publication: Houston, TX

Publisher: MD2B

Publication Date: 2011

Physical Description: Paperback, 420 p.

Subject: Leadership/Coaching; Administration

Abstract: The book begins as a how-to guide, with clerkship-specific templates, such as op notes and admission orders, along with sample notes and guides for every aspect of core clerkships (internal medicine, surgery, pediatrics, obstetrics/gynecology, psychiatry, family medicine). The book reviews proven strategies for success in patient care, write-ups, rounds, and other vital areas. Grades in required rotations are the most important academic criteria used to select residents, and this critical year can determine career choices as well. This book shows students what they can do now to position themselves for match success. An invaluable resource for medical students - no student should be without it.

ISBN: 9780972556194

Language: English

Material Type: Book

Call Number: REF AA 500 DES 2011

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Before We Are Born:: Essentials of Embryology and Birth Defects

https://cwslc.andornot.com/en/permalink/catalog125205

Wynbrandt, James., Ludman, Mark D. New York, NY: Elsevier Canada , 2019. 10th.

Material Type: Book

Call Number: REF GI 200 MOO 2019

Availability: 1 copy, 1 available

Covering the essentials of normal and abnormal human development for students in a variety of health science disciplines,Before We Are Born: Essentials of Embryology and Birth Defects, 10th Edition,reflects new research findings and current clinical practice through concise text and abundant illust…

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Author: Wynbrandt, James.; Ludman, Mark D.

Edition: 10th

Place of Publication: New York, NY

Publisher: Elsevier Canada

Publication Date: 2019

Physical Description: Hardcover, 350 pp.

Subject: Genetics/Genetic Disorders-Encyclopedias; Genetic Disorders; Birth Defects. Congenital Abnormalities; Children's Health-Encyclopedias; UBC MD Undergrad

Abstract: Covering the essentials of normal and abnormal human development for students in a variety of health science disciplines,Before We Are Born: Essentials of Embryology and Birth Defects, 10th Edition,reflects new research findings and current clinical practice through concise text and abundant illustrations . This edition has been fully updated by the world's foremost embryologists and is based on the popular text,The Developing Human, written by the same author team. It provides an easily accessible understanding of all of the latest advances in embryology, includingnormal and abnormal embryogenesis, causes of birth defects, and the role of genes in human development.

ISBN: 978-0323608497

Language: English

Material Type: Book

Call Number: REF GI 200 MOO 2019

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Revise Search

Smith's recognizable patterns of human malformation

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Learning as a way of being: Strategies for survival in a world of permanent white water

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Now, discover your strengths

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Quiet leadership: Help people think better -- don't tell them what to do: Six steps to transforming performance at work

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Creating a culture of collaboration

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Websites

The handbook of leadership development evaluation

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Encyclopedia of genetic disorders and birth defects

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Patients come second: Leading change by changing the way you lead

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A guide to the project management body of knowledge: PMBOK (R) Guide

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Success on the wards: 250 rules for clerkship success

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Before We Are Born:: Essentials of Embryology and Birth Defects

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