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

Copies

Website

http://www.ncbi.nlm.nih.gov/omim

Website Notes

The database corresponds to the print publication.

Author

McKusiak, Victor A (Ed).

Edition

12th Ed.

Place of Publication

Baltimore, MD

Publisher

Johns Hopkins University Press

Publication Date

1998

Physical Description

Hardcover

Subject

Genetics

Genetic Disorders

Genetics/Genetic Disorders-Encyclopedias

Abstract

A comprehensive, authoritative and timely knowledgebase of human genes and genetic disorders compiled to support human genetics research and education and the practice of clinical genetics.

ISBN

0801857422

Language

English

Material Type

Book

Call Number

REF GI 20 MCK 1998 VOL 1

Copies

Website

http://www.ncbi.nlm.nih.gov/omim

Website Notes

The database corresponds to the print publication.

Author

McKusiak, Victor A (Ed).

Edition

12th Ed.

Place of Publication

Baltimore, MD

Publisher

Johns Hopkins University Press

Publication Date

1998

Physical Description

Hardcover

Subject

Genetics

Genetics/Genetic Disorders-Encyclopedias

Genetic Disorders

Abstract

A comprehensive, authoritative and timely knowledgebase of human genes and genetic disorders compiled to support human genetics research and education and the practice of clinical genetics.

ISBN

0801857422

Language

English

Material Type

Book

Call Number

REF GI 20 MCK 1998 VOL 2

Copies

Website

http://www.ncbi.nlm.nih.gov/omim

Website Notes

The database corresponds to the print publication.

Author

McKusiak, Victor A (Ed).

Place of Publication

Baltimore, MD

Publisher

Johns Hopkins University Press

Publication Date

1998

Physical Description

Hardcover

Subject

Genetic Disorders

Genetics

Genetics/Genetic Disorders-Encyclopedias

Abstract

A comprehensive, authoritative and timely knowledgebase of human genes and genetic disorders compiled to support human genetics research and education and the practice of clinical genetics.

ISBN

0801857422

Language

English

Material Type

Book

Call Number

REF GI 20 MCK 1998 VOL 3

Copies

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

Copies

Author

Ness, Bryan D. (ed.)

Knight, Jeffrey A. (ed.)

Edition

Revised Edition

Place of Publication

Pasadena, Ca.

Publisher

Salem Press, Inc.

Publication Date

2004

Physical Description

Hardcover: 440 p.

Subject

Genetics

Genetics/Genetic Disorders-Encyclopedias

UBC MD Undergrad

Abstract

This encyclopedia provides a thorough yet accessible overview of genetics. This revised edition adds 64 new overview essays to the 172 original entries.

ISBN

1587651491

Language

English

Material Type

Book

Call Number

REF GI 20 NES 2004 v.1

Copies

Author

Ness, Bryan D. (ed.)

Knight, Jeffrey A. (ed.)

Edition

Revised Edition

Place of Publication

Pasadena, Ca.

Publisher

Salem Press, Inc.

Publication Date

2004

Physical Description

Hardcover: 863 p.

Subject

Genetics

Genetics/Genetic Disorders-Encyclopedias

UBC MD Undergrad

Abstract

This encyclopedia provides a thorough yet accessible overview of genetics. This revised edition adds 64 new overview essays to the 172 original entries.

ISBN

1587651491

Language

English

Material Type

Book

Call Number

REF GI 20 NES 2004 v.2

Copies

Author

Milunsky, Aubrey (ed.)

Milunsky, Jeff M. (ed.)

Edition

6th ed.

Place of Publication

Hoboken, NJ

Publisher

Wiley-Blackwell

Publication Date

2010

Physical Description

Hardcover: 1135 p.

Subject

Genetic Disorders

Genetics

UBC MD Undergrad

Abstract

This text is in its 6th edition as a major repository of facts about prenatal diagnosis. It is an essential resource for all engaged in prenatal genetic diagnosis, especially obstetricians, maternal-fetal medicine specialists, medical geneticists, genetic counsellors, and pediatricians.

ISBN

9781405190879

Language

English

Material Type

Book

Call Number

REF GI 300 MIL 2010

Copies

Author

Gupta, Piyush

Menon, PSN

Ramji, Siddarth

Lodha, Rakesh

Edition

1st

Place of Publication

New Delhi, India

Publisher

JP Medical Publishers

Publication Date

2018

Physical Description

977 pp

Subjects

Infections

Pediatrics

Systemic Disorders

Subject

Children's Health. Pediatrics

UBC MD Undergrad

Abstract

Postgraduate Textbook of Pediatricsis a comprehensive guide to paediatrics. The textbook is comprised of three volumes, split into ten parts with over 600 chapters, and contributions from over 50 section editors and 725 authors, covering all paediatric disorders, descriptions of diseases and their management. The second volume covers infections and systemic diseases, featuring a range of infections from bacterial, to viral and fungal, and systemic disorders including gastrointestinal, respiratory and cardiovascular. Postgraduate Textbook of Pediatricsincludes nearly 1500 images and illustrations in full colour, incorporating information on modern imaging techniques for neurological disorders in children. The textbook also includes appendices for laboratory values and drug doses. This is an ideal resource for postgraduate students to gain a firm grounding in, and retain and improve their knowledge of all areas of paediatric medicine. Key Points Second volume of comprehensive, three volume guide to paediatrics 3 volumes feature over 50 section editors and 725 contributing authors 1479 full colour images and illustrations

ISBN

978-9351529552

Language

English

Material Type

Book

Call Number

REF GK 100 GUP 2018 V2

Copies

Author

Harper, Peter S.

Edition

7th ed.

Place of Publication

London, UK

Publisher

Hodder Arnold

Publication Date

2010

Physical Description

Softcover: 393 p.

Subject

Genetics

Genetic Counseling

UBC MD Undergrad

Abstract

This guide serves as a reference for professionals who are counselling those at risk from inherited disorders. It contains information on: developments in common disease genetics, new molecular techniques and genetic counselling, non invasive prenatal diagnosis, the molecular basis of congenital malformations, the history of genetic counselling and the social and ethical aspects of advances in genetics.

ISBN

9780340990698

Language

English

Material Type

Book

Call Number

REF GI 250 HAR 2010

Copies

Author

Gupta, Piyush

Menon, PSN

Ramji, Siddarth

Lodha, Rakesh

Place of Publication

New Delhi, India

Publisher

JP Medical Publishers

Publication Date

2018

Physical Description

977 pp

Subjects

Social Pediatrics

Pediatrics

Systemic Disorders

Subject

Children's Health. Pediatrics

UBC MD Undergrad

Abstract

Postgraduate Textbook of Pediatricsis a comprehensive guide to paediatrics. The textbook is comprised of three volumes, split into ten parts with over 600 chapters, and contributions from over 50 section editors and 725 authors, covering all paediatric disorders, descriptions of diseases and their management. The third volume covers systemic disorders further, including neurological, eye and skin disorders. This volume also covers social paediatrics including sections on vulnerable children and community paediatrics. Postgraduate Textbook of Pediatricsincludes nearly 1500 images and illustrations in full colour, incorporating information on modern imaging techniques for neurological disorders in children. The textbook also includes appendices for laboratory values and drug doses. This is an ideal resource for postgraduate students to gain a firm grounding in, and retain and improve their knowledge of all areas of paediatric medicine. Key Points Third volumed of comprehensive, three volume guide to paediatrics Complete textbook features 50 section editors and 725 contributing authors 1479 full colour images and illustrations

ISBN

978-9351529569

Language

English

Material Type

Book

Call Number

REF GK 100 GUP 2018 V3

Copies

Author

American Psychiatric Association

Edition

5th ed.

Place of Publication

Arlington, VA

Publisher

American Psychiatric Association

Publication Date

2013

Physical Description

xliv, 947 p. ; 26 cm.

Subject

Mental Disorders-Diagnosis

Mental Disorders-Therapy

UBC MD Undergrad

Abstract

This is the standard reference for clinical practice in the mental health field. The disorders included in DSM-5 were reordered into a revised organizational structure meant to stimulate new clinical perspectives. This new structure corresponds with the organizational arrangement of disorders planned for ICD-11 scheduled for release in 2015. Other enhancements have been introduced to promote ease of use across all settings, including: Representation of developmental issues related to diagnosis; Integration of scientific findings from the latest research in genetics and neuroimaging; Consolidation of autistic disorder, Asperger's disorder, and pervasive developmental disorder into autism spectrum disorder; Streamlined classification of bipolar and depressive disorders; Restructuring of substance use disorders for consistency and clarity; Enhanced specificity for major and mild neurocognitive disorders; Transition in conceptualizing personality disorders; New disorders and features; Online enhancements.

ISBN

9780890425558

Language

English

Material Type

Book

Call Number

REF CD 140 AME 2013

Copies

Author

Maheu, Louis

Macdonal, Roderick A. (Eds)

Place of Publication

Kingston, ON

Publisher

McGill-Queen's University Press

Publication Date

2011

Physical Description

319 pages

Subject

Personality

Genetics

UBC MD Undergrad

Abstract

Advances in genetic research have captured the attention of the media and the public through reports about genetically caused diseases and behaviours. However, all too often the coverage of scientists' innovations has implied that genetic factors alone are responsible for effects ranging from personality and sexual preferences to morbid obesity and intellectual disabilities. Challenging Genetic Determinism argues that hypotheses cannot be based solely on genetic factors but must take into account the context in which these factors occur.

ISBN

978-0773538139

Language

English

Material Type

Book

Call Number

REF GI 200 MAC 2011

Copies

Author

Posner, Glenn D

Dy, Jessica

Black, Amanda Y

Jones, Griffith D

Edition

6th Ed.

Place of Publication

New York

Publisher

McGraw Hill

Publication Date

2013

Physical Description

Softcover: 782 pages

Subject

Embryology

Labor Birth

Abstract

Edition after acclaimed edition, Oxorn-Foote Human Labor & Birth has provided the most comprehensive, yet accessible overview of obstetrics available. Going beyond scientific theory and a technological orientation, this landmark guide is written for the real world of clinical practice, as it expertly examines all mechanisms of human labor and delivery.

The book begins with a valuable review of clinical anatomy, then thoroughly examines the three stages of labor, with a focus on proper management and birthing techniques. Specific guidance on the full spectrum of complications and delivery situations, including Cesareansection, breech presentation, transverse lie, umbilical cord issues, dystocia, and more are also presented. A final section addresses such critical concerns as preterm labor, antepartum hemorrhage, and maternal and fetal complications in labor.

ISBN

9780007-1740289

Language

English

Material Type

Book

Call Number

REF AB 56 POS 2013

Copies

Author

O'Toole, Marie T. (ed.)

Allegrante, John (ed.)

Cortese, Bernard (ed.)

Hamric, Ann B. (ed.)

Hinojosa, Jim (ed.)

Jones, Patricia S. (ed.)

Kay, Elizabeth (ed.)

Nussbaum, Burton (ed.)

O'Donnell, Edmond F. (ed.)

Edition

7th ed.

Place of Publication

Philadelphia, PA

Publisher

Saunders

Publication Date

2003

Physical Description

Hardcover: 2259 p.

Subject

Medical Encyclopedias

Medical Dictionaries. Medical Thesauri. Medical Terminology

Abstract

Encyclopedic entries are included for significant topics, such as diseases, disorders, or conditions. These encyclopedic entries include the definition along with an overview of the most important information related to Symptoms, Treatment, Patient Care, Prevention, etc.

ISBN

9780721697918

Language

English

Material Type

Book

Call Number

REF AB 20 OTO 2003

Copies

Website

http://hdl.handle.net/2429/1228

Author

Ferguson, Kyle Akira

Place of Publication

[Vancouver, BC?]

Publisher

University of British Columbia

Publication Date

2008

Subject

Faculty of Medicine

Theses

Abstract

While the introduction of intracytoplasmic sperm injection (ICSI) has revolutionized the treatment of male infertility, concerns have been raised regarding the risk of chromosomal abnormalities in pregnancies derived from ICSI. Studies on sperm from infertile men have suggested that this population may produce higher rates of aneuploid sperm. Thus, we hypothesized that defects in early meiotic events may contribute to both male infertility and the production of aneuploid sperm.

Language

English

Material Type

Thesis

Call Number

Thesis Shelf

Author

Black, Donald

Andreasen, Nancy

Edition

6th ed.

Place of Publication

Arlington, VA

Publisher

American Psychiatric Publishing

Publication Date

2014

Subject

Mental Health/Illness

Mental Disorders

UBC MD Undergrad

Abstract

The book provides an introduction to the field both for students new to psychiatry and for students who are studying for their board exams. Chief among these was the publication of DSM-5(R), which necessitated a complete restructuring of the text, the reformulation of many diagnostic categories, and the addition of new disorders.

ISBN

9781585624690

Language

English

Material Type

Book

Call Number

REF CD 05 BLA 2014

Copies

Author

Sadock, Benjamin

Sadock, Virginia

Ruiz, Pedro

Edition

11th ed.

Place of Publication

Philadelphia, PA

Publisher

Wolters Kluwer

Publication Date

2015

Physical Description

xvi, 1472 pages ; 27 cm

Subject

Mental Health/Illness

Mental Disorders

UBC MD Undergrad

Abstract

The goal of this book is to foster professional competence and ensure high quality care to those with mental illness. An eclectic, multidisciplinary approach has been its hallmark; thus, biological, psychological, and sociological factors are equitably presented as they affect the person in health and disease.

ISBN

9781609139711

Language

English

Material Type

Book

Call Number

REF CD 05 SAD 2015

Copies

Author

Nussbaum, Robert L.

McInnes, Roderick R.

Willard, Huntington F.

Hamosh, Ada

Edition

7th ed.

Place of Publication

Philadelphia, PA

Publisher

Saunders Elsevier

Publication Date

2007

Physical Description

Softcover: 566 p.

Subject

Genetics

UBC MD Undergrad

Abstract

This text integrates the classic principles of human genetics with modern molecular genetics to help you diagnose and manage a wide range of genetic disorders.

ISBN

97814116030805

Language

English

Material Type

Book

Call Number

REF GI 200 NUS 2007

Copies

Author

Rimoin, David L.

Pyeritz, Reed E.

Korf, Bruce R. (Eds).

Edition

5th Ed.

Place of Publication

Philadelphia, PA

Publisher

Churchill Livingstone Elsevier

Publication Date

2007

Physical Description

Hardcover: 1082 pages

Subject

Genetics

UBC MD Undergrad

Abstract

This 3 volume text emphasizes application as well as the theory of medical genetics across the full spectrum of inherited disorders. Get expert clinical advice and guidance from over 250 of the world's most trusted authorities in medical genetics.

Volume 1 covers: Basic principles; General principles; Approaches to clinical problems; Approaches to specific disorders.

ISBN

9780443068706

Language

English

Material Type

Book

Call Number

REF GI 200 RIM 2007 VOL 1

Copies