Clinical, cytogenetic, and molecular characterization of six patients with ring chromosomes 22, including one with concomitant 22q11.2 deletion-Reference-Cited by-同舟云学术

Clinical, cytogenetic, and molecular characterization of six patients with ring chromosomes 22, including one with concomitant 22q11.2 deletion

Published:2014-04-03 Issue:7 Volume:164 Page:1659-1665
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Guilherme Roberta Santos¹,Soares Karina Cunha²,Simioni Milena²,Vieira Tarsis Paiva²,Gil-da-Silva-Lopes Vera Lúcia²,Kim Chong Ae³,Brunoni Décio¹,Spinner Nancy Bettina⁴,Conlin Laura Kathleen⁴,Christofolini Denise Maria⁵,Kulikowski Leslie Domenici⁶,Steiner Carlos Eduardo²,Melaragno Maria Isabel¹

Affiliation:

1. Genetics Division, Department of Morphology and Genetics; Universidade Federal de São Paulo; São Paulo Brazil

2. Department of Medical Genetics; Universidade Estadual de Campinas (UNICAMP); Campinas SP Brazil

3. Department of Pediatrics, Instituto da Criança HC-FMUSP; Universidade de São Paulo; São Paulo Brazil

4. Department of Pathology, Children's Hospital of Philadelphia, and the Perelman School of Medicine; The University of Pennsylvania; Philadelphia Pennsylvania

5. Gynecology and Obstetrics Division; Faculdade de Medicina do ABC; São Paulo Brazil

6. Department of Pathology, Laboratório de Citogenômica; Universidade de São Paulo; São Paulo Brazil

Funder

FAPESP, Brazil

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.36512/fullpdf

Reference33 articles.

1. FISH-mapping of a 100-kb terminal 22q13 deletion;Anderlid;Hum Genet,2002