Clinical genetics evaluation in identifying the etiology of autism spectrum disorders
- 1 April 2008
- journal article
- practice guideline
- Published by Elsevier BV in Genetics in Medicine
- Vol. 10 (4), 301-305
- https://doi.org/10.1097/gim.0b013e31816b5cc9
Abstract
No abstract availableKeywords
This publication has 37 references indexed in Scilit:
- Chromosome 2q37 deletion: Clinical and molecular aspectsAmerican Journal Of Medical Genetics Part C-Seminars In Medical Genetics, 2007
- Duplication of 17(p11.2p11.2) in a male child with autism and severe language delayAmerican Journal of Medical Genetics Part A, 2007
- Array-based comparative genomic hybridisation identifies high frequency of cryptic chromosomal rearrangements in patients with syndromic autism spectrum disordersJournal of Medical Genetics, 2006
- Genetic landmarks through philately – autism spectrum disorders: a genetic updateClinical Genetics, 2004
- Etiologic Yield of Autistic Spectrum Disorders: A Prospective StudyJournal of Child Neurology, 2001
- Linkage-Disequilibrium Mapping of Autistic Disorder, with 15q11-13 MarkersAmerican Journal of Human Genetics, 1998
- Smith-Magenis syndrome resulting from a de novo direct insertion of proximal 17q into 17p11.2American Journal of Medical Genetics, 1998
- Chromosomes in autism and related pervasive developmental disorders: a cytogenetic studyJournal of Intellectual Disability Research, 1998
- Autistic disorder in Sotos syndrome: A case reportEuropean Journal of Pediatrics, 1990
- Fragile X in a Survey of 75 Autistic MalesNew England Journal of Medicine, 1984