Neurogenetic developmental disorders variation of manifestation in childhood (MIT Press, 2007)
Includes bibliographical references and index
Turner syndrome in childhood - Marsha L. Davenport, Stephen R. Hooper and Martha Zeger -- - Klinefelter syndrome - Judith L. Ross, Gerry A. Stefanatos and David Roeltgen -- - Fragile X syndrome : the journey from genes to behavior - Kimberly M. Cornish, Andrew Levitas and Vicki Sudhalter -- - Duchenne muscular dystrophy - Veronica J. Hinton and Edward M. Goldstein -- - Neurofibromatosis - John M. Slopis and Bartlett D. Moore III -- - Cognitive and behavioral characteristics of children with chromosome 22q11.2 deletion syndrome - Tony J. Simon, Merav Burg-Malki and Doron Gothelf -- - Williams Syndrome - Carolyn B. Mervis and Colleen A. Morris -- - Congenital hypothyroidism : genetic and biochemical influences on brain development and neuropsychological functioning - Joanne F. Rovet and Rosalind Brown -- - Inborn errors of metabolism - Kevin M. Antshel and Georgianne Arnold -- - Neurodevelopmental effects of childhood exposure to heavy metals : lessons from pediatric lead poisoning - Theodore I. Lidsky, Agnes T. Heaney, Jay S. Schneider and John F. Rosen -- - Beyond the diagnosis : the process of genetic counseling - Allyn McConkie-Rosell and Julianne O'Daniel -- - From diagnosis to adaptation : optimizing family and child functioning when a genetic diagnosis is associated with mental retardation - Laraine Masters Glidden and Sarah A. Schoolcraft -- - When a genetic disorder is associated with learning disabilities - Michele M. M. Mazzocco -- - Early intervention and early childhood special education for young children with neurogenetic disorders - Deborah D. Hatton -- - The individualized education program : navigating the IEP development process - Vicki Sudhalter