Eric Engel and Stylianos Antonarakis have written the most authoritative and vital reference on molecular and clinical aspects of uniparental disomy (UPD) and genomic imprinting to date. Genomic Imprinting and Uniparental Disomy in Medicine features comprehensive overviews of a multitude of genetic disorders linked to UPD, with a strong emphasis on clinical consequences. This book will provide readers with the tools necessary to identify and treat diseases associated with nontraditional chromosomal inheritance.
Genomic Imprinting and Uniparental Disomy in Medicine features handy tables summarizing clinical phenotypes and chromosomal involvement in UPD, as well as clear illustrations on imprinting mechanisms and diagnostic testing. This authoritative, completely up-to-date practical reference will be useful for any clinical geneticist, genetic counselor, physician, or researcher encountering patients with such disorders or studying complex disease mechanisms.
Rezensionen / Stimmen
"...a thorough review...a great...reference..." (Journal of Genetic Counseling, Vol. 12, No. 3, June 2003)
Sprache
Verlagsort
Verlagsgruppe
Zielgruppe
Für höhere Schule und Studium
Für Beruf und Forschung
Maße
Höhe: 245 mm
Breite: 162 mm
Dicke: 20 mm
Gewicht
ISBN-13
978-0-471-35126-9 (9780471351269)
Copyright in bibliographic data and cover images is held by Nielsen Book Services Limited or by the publishers or by their respective licensors: all rights reserved.
Schweitzer Klassifikation
Eric Engel M.D. is Honorary Professor of Medicine at the Geneva University School of Medicine in Geneva, Switzerland. He received his M.D. from the Geneva University School of Medicine in 1951. In the course of his career he has been a Research Fellow and Instructor of Medicine, Harvard Medical School, Professor of Medicine and head of the Genetic Center, Vanderbilt University School of Medicine, and finally, Professor of Medicine and Director of The Medical Institute of Genetics, Geneva University.
Autor*in
Division of Medical Genetics, University of Geneva Medical School, Switzerland
Division of Medical Genetics, University of Geneva Medical School, Switzerland
Foreword.
Preface.
Acknowledgements.
Introduction.
Detection of Uniparental Disomy and Imprinting by DNA Analysis.
Mechanisms Generating Uniparently Disomy and Genomic ImprintingDisorders.
Uniparental Disomy for Individual Human Chromosomes: Review ofCases.
"Old" and "New" Syndromes with Uniparental Disomy.
The Prader-(Labhardt)-Willi Syndrome.
The Angelman Syndrome (AS).
The Beckwith-Wiedemann Syndrome (BWS).
Genetic Counseling and Prenatal Diagnosis.
Genomic Imprinting in the Mouse.
Epilogue of an Unfinished Story.
Index.
