SOX12andNRSN2are candidate genes for 20p13 subtelomeric deletions associated with developmental delay-Reference-Cited by-同舟云学术

SOX12andNRSN2are candidate genes for 20p13 subtelomeric deletions associated with developmental delay

Published:2013-09-06 Issue:8 Volume:162 Page:832-840
ISSN:1552-4841
Container-title:American Journal of Medical Genetics Part B: Neuropsychiatric Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

An Yu¹²,Amr Sami S.³⁴⁵,Torres Alcy³⁶,Weissman Laura³⁷,Raffalli Peter³⁶,Cox Gerald³⁸,Sheng Xiaoming²,Lip Va²,Bi Weimin⁹,Patel Ankita⁹,Stankiewicz Pawel⁹,Wu Bai-Lin¹²³,Shen Yiping²³¹⁰

Affiliation:

1. Institutes of Biomedical Sciences; Children's Hospital and MOE Key Laboratory of Contemporary Anthropology; Fudan University; Shanghai China

2. Department of Laboratory Medicine; Boston Children's Hospital; Boston Massachusetts

3. Harvard Medical School; Boston Massachusetts

4. Brigham and Woman's Hospital; Boston Massachusetts

5. Partners Healthcare Center for Personalized Genetic Medicine; Cambridge Massachusetts

6. Department of Neurology; Boston Children's Hospital; Boston Massachusetts

7. Developmental Medicine Center; Boston Children's Hospital; Massachusetts

8. Genetics Program; Boston Children's Hospital, Boston; Massachusetts

9. Department of Molecular and Human Genetics; Baylor College of Medicine; Houston Texas

10. Shanghai Children's Medical Center; Jiaotong University School of Medicine; Shanghai China

Publisher

Wiley

Subject

Cellular and Molecular Neuroscience,Psychiatry and Mental health,Genetics(clinical)

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.b.32187/fullpdf

Reference21 articles.

1. Study of 250 children with idiopathic mental retardation reveals nine cryptic and diverse subtelomeric chromosome anomalies;Baker;Am J Med Genet Part A,2002

2. Organogenesis relies on SoxC transcription factors for the survival of neural and mesenchymal progenitors;Bhattaram;Nat Commun,2010

3. Detection of clinically relevant exonic copy-number changes by array CGH;Boone;Hum Mutat,2010

4. del(20p) with manifestations of arteriohepatic dysplasia;Byrne;Am J Med Genet,1986

5. The three SoxC proteins-Sox4, Sox11 and Sox12-exhibit overlapping expression patterns and molecular properties;Dy;Nucleic Acids Res,2008

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