Deletion 2q37 syndrome: Cognitive-behavioral trajectories and autistic features related to breakpoint and deletion size-Reference-Cited by-同舟云学术

Deletion 2q37 syndrome: Cognitive-behavioral trajectories and autistic features related to breakpoint and deletion size

Published:2016-06-09 Issue:9 Volume:170 Page:2282-2291
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Fisch Gene S.¹,Falk Rena E.²,Carey John C.³,Imitola Jaime⁴,Sederberg Maria⁵⁶,Caravalho Karen S.⁷,South Sarah³⁶

Affiliation:

1. Department of Statistics and CIS; CUNY/Baruch College; New York New York

2. Cedar Sinai Hospital; Los Angeles California

3. Department of Pediatrics; University of Utah; Salt Lake City Utah

4. Laboratory of Neural Stem Cells and Functional Neurogenetics, Department of Neurology and Neuroscience; The Ohio State University; Columbus Ohio

5. Department of Pathology; University of Utah; Salt Lake City Utah

6. ARUP Institute for Research and Experimental Pathology; Salt Lake City Utah

7. Section of Pediatric Neurology, St. Christopher Hospital for Children; Drexel University College of Medicine; Philadelphia Pennsylvania

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference39 articles.

1. Molecular analysis of 20 patients with 2q37.3 monosomy: Definition of minimum deletion intervals for key phenotypes;Aldred;J Med Genet,2004

2. Familial cryptic translocation between chromosomes 2qter and 8qter: Further delineation of the Albright hereditary osteodystrophy-like phenotype;Bijlsma;J Med Genet,1999

3. A cryptic deletion of 2q35 including part of the PAX3 gene detected by breakpoint mapping in a child with autism and a de novo 2;8 translocation;Borg;J Med Genet,2002

4. Partial 6p trisomy associated with infantile autism;Burd;Clin Genet,1988

5. Evidence for a susceptibility gene for autism on chromosome 2 and for genetic heterogeneity;Buxbaum;Am J Hum Genet,2001

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