Savant Characteristics in a Child with Developmental Delay and Deletion in the Short Arm of Chromosome 20-Reference-Cited by-同舟云学术

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Savant Characteristics in a Child with Developmental Delay and Deletion in the Short Arm of Chromosome 20

Published:2008-11-12 Issue:7 Volume:37 Page:637-644
ISSN:0012-1622
Container-title:Developmental Medicine & Child Neurology
language:en
Short-container-title:

Author:

Rovet J.,Krekewich K.,Perlman K.,Weksberg R.,Holland J.,Feigenbaum A.

Publisher

Wiley

Subject

Clinical Neurology,Developmental Neuroscience,Pediatrics, Perinatology, and Child Health

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1469-8749.1995.tb12052.x/fullpdf

Reference50 articles.

1. Alagille syndrome and dele-lion of 20p;Anad;Journal of Medical Genetics.,1990

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2. Delineation of a region responsible for panhypopituitarism in 20p11.2;American Journal of Medical Genetics Part A;2013-05-08

3. The Savant Syndrome and Its Possible Relationship to Epilepsy;Advances in Experimental Medicine and Biology;2012

4. 20p11 deletion in a female child with panhypopituitarism, cleft lip and palate, dysmorphic facial features, global developmental delay and seizure disorder;American Journal of Medical Genetics Part A;2010-12-28

5. A tale of two deletions: A report of two novel 20p13 → pter deletions;American Journal of Medical Genetics Part A;2010-04

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