Providing a comprehensive survey of the clinical, educational, developmental, psychosocial, and transitional issues relevant to people with Down syndrome, this book addresses the needs of family members, caregivers, and professionals alike. Edited in association with the National Down Syndrome Society, this up-to-date treatment incorporates the newest developments concerning sexuality, inclusion, transition into adulthood, and legislation, as well as a discussion of the Human Genome Project and the sequencing of chromosome 21.
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"This volume is a comprehensive collection of articles representing a wide range of disciplines it will be a valuable addition to the bookshelves of families, medical staff, educators, and researchers." (American Journal of Medical Genetics, August 15, 2004) "This book will be of great interest to anyone wanting to have the latest information about this genetic disorder..." (www.family2000.org.uk, 9 September 2002) "...puts foward some of the visions and thoughts in an optimistic way and is therefore recommended..." (Int Jnl of Adolescent Medical Health) "...puts forward some of the visions and thoughts in an optimistic way and is therefore recommended..." (Int Jnl of Adolescent Medical Health, Vol.15, No.1, 2003) "I...consider a copy of this book a must for every institutional and personal library." (Journal of the National Medical Association, March 2003) "...exceedingly valuable for a wide spectrum of individuals: parents, professionals, caregivers, and researchers..." (American Journal of Human Genetics, Vol. 72, 2003) "...exceedingly valuable for a wide spectrum of individuals: parents, professionals, caregivers, and researchers..." (American Journal of Human Genetics, Vol. 72, 2003) "...a terrific compendium of the wide array of topics...whatever the challenges that lie ahead...we are much better prepared by the information and vision provided by this excellent book." (Archives of Pediatrics and Adolescent Medicine, May 2003) "...a useful reference tool for families and service providers." (Human Genetics, No.113, 2003)