Expanding the genotype-phenotype correlation in subtelomeric 19p13.3 microdeletions using high resolution clinical chromosomal microarray analysis-Reference-Cited by-同舟云学术

Expanding the genotype-phenotype correlation in subtelomeric 19p13.3 microdeletions using high resolution clinical chromosomal microarray analysis

Published:2013-10-02 Issue:12 Volume:161 Page:2953-2963
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Peddibhotla Sirisha¹²,Khalifa Mohamed³,Probst Frank J.¹,Stein Jennifer³,Harris Leslie L.⁴,Kearney Debra L.⁵,Vance Gail H.⁶,Bull Marilyn J.⁷,Grange Dorothy K.⁸,Scharer Gunter H.⁹¹⁰,Kang Sue-Hae L.¹¹,Stankiewicz Pawel¹,Bacino Carlos A.¹,Cheung Sau W.¹,Patel Ankita¹

Affiliation:

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

2. Department of Pediatrics-Hematology-Oncology; Baylor College of Medicine and Texas Children's Cancer Center; Houston, Texas

3. Department of Genetics; Akron Children's Hospital; Akron, Ohio

4. Department of Pediatrics; Baylor College of Medicine and Texas Children's Hospital; Houston, Texas

5. Department of Pathology and Immunology; Baylor College of Medicine and Texas Children's Hospital; Houston, Texas

6. Department of Medicine and Molecular Genetics; Indiana University School of Medicine; Indianapolis, Indiana

7. Section of Developmental Pediatrics; Riley Hospital for Children at IU Health; Indianapolis, Indiana

8. Division of Genetics and Genomic Medicine; Department of Pediatrics; Washington University School of Medicine; St. Louis Children's Hospital; St. Louis, Missouri

9. Division of Clinical Genetics & Metabolism; Department of Pediatrics; University of Colorado School of Medicine; Aurora, Colorado

10. CHW Genetics Center; Medical College of Wisconsin; Milwaukee WI

11. Allina Medical Laboratories; Minneapolis, Minnesota

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.35886/fullpdf

Reference15 articles.

1. Molecular characterization of a novel, de novo, cryptic interstitial deletion on 19p13.3 in a child with a cutis aplasia and multiple congenital anomalies;Al-Kateb;Am J Med Genet Part A,2010

2. Distinct phenotype associated with a cryptic subtelomeric deletion of 19p13.3-pter;Archer;Am J Med Genet Part A,2005