| Description |
1 online resource (xiv, 507 pages) : illustrations. |
| Physical Medium |
polychrome |
| Description |
text file |
| Series |
Issues in clinical and cognitive neuropsychology
|
|
Issues in clinical and cognitive neuropsychology.
|
| Bibliography |
Includes bibliographical references and index. |
| Contents |
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 -- Individualized education program : navigating the IEP development process / Vicki Sudhalter. |
| Summary |
A reference to guide clinicians, researchers, teachers, and parents in identifying a range of genetic disorders despite widely variable cognitive, behavioral, and physical effects. |
| Local Note |
eBooks on EBSCOhost EBSCO eBook Subscription Academic Collection - North America |
| Subject |
Developmental disabilities -- Genetic aspects.
|
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Developmental disabilities -- Genetic aspects. |
|
Developmental disabilities. |
|
Chromosome abnormalities.
|
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Chromosome abnormalities. |
|
Neurogenetics.
|
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Neurogenetics. |
|
Pediatric neuropsychology.
|
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Pediatric neuropsychology. |
|
Genetic Diseases, Inborn -- diagnosis. |
|
Child. |
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Genetic Counseling -- methods. |
|
Heredodegenerative Disorders, Nervous System -- diagnosis. |
|
Sex Chromosome Disorders -- diagnosis. |
| Genre/Form |
Electronic books.
|
| Added Author |
Mazzocco, Michèle M. M.
|
|
Ross, Judith L.
|
| Other Form: |
Print version: Neurogenetic developmental disorders. Cambridge, Mass. : MIT Press, ©2007 9780262134804 0262134802 (DLC) 2006046910 (OCoLC)73994340 |
| ISBN |
9780262279321 (electronic book) |
|
0262279320 (electronic book) |
|
9781429477154 (electronic book) |
|
1429477156 (electronic book) |
|
1282098853 |
|
9781282098855 |
|
9780262134804 (hc ; alkaline paper) |
|
0262134802 (hc ; alkaline paper) |
|
