The Fragile X Syndrome
Diagnosis, Treatment and Research
Johns Hopkins University Press
2nd Edition
Published on 19. June 1996
Book
Hardback
384 pages
978-0-8018-5388-3 (ISBN)
Article exhausted; check for reprint
Description
This new edition of 'Fragile X Syndrome' includes updated information on the latest research findings--especially in molecular biology--as well as new photographs highlighting clinical features and thorough coverage of treatment and intervention, diagnosis, and research. 'Praise for the first edition:' "Answers nearly all the questions that parents or clinicians might raise about fragile X syndrome...Can be recommended confidently as a thoroughly up-to-date, reliable, and informative account of the condition."--'Lancet' "The clinical and cytogenetic material in this book is excellent and provides a strong background for physicians and students...'Fragile X Syndrome' still presents the best comprehensive treatment of this complex disorder. Physicians, students, and other interested professionals can either read this book from cover to cover or select the chapters that interest or apply to them."--'New England Journal of Medicine'
More details
Edition
2nd Revised edition
Language
English
Place of publication
Baltimore, MD
United States
Target group
College/higher education
Professional and scholarly
Edition type
Revised edition
Illustrations
76ill.
Dimensions
Height: 230 mm
Weight
800 gr
ISBN-13
978-0-8018-5388-3 (9780801853883)
Copyright in bibliographic data is held by Nielsen Book Services Limited or its licensors: all rights reserved.
Schweitzer Classification
Other editions
New editions

Book
07/2002
3rd Edition
Johns Hopkins University Press
€62.00
Article not available for order
Persons
Randi Jenssen Hagerman, M.D., is associate professor of pediatrics at the University of Colorado Health Science Center. Amy Cronister, M.S., is a genetics counselor.