Interstitial 10p deletion derived from a maternal ins(16;10)(q22;p13p15.2): Report of the first familial case of 10p monosomy affecting to two familial members of different generations-Reference-Cited by-同舟云学术

Interstitial 10p deletion derived from a maternal ins(16;10)(q22;p13p15.2): Report of the first familial case of 10p monosomy affecting to two familial members of different generations

Published:2016-01-14 Issue:5 Volume:170 Page:1268-1273
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Fernández Raquel M.¹²,Sánchez Javier¹²,García-Díaz Lutgardo¹,Peláez-Nora Yolanda¹,González-Meneses Antonio³,Antiñolo Guillermo¹²,Borrego Salud¹²

Affiliation:

1. Department of Genetics; Reproduction and Fetal Medicine; Institute of Biomedicine of Seville (IBIS); University Hospital Virgen del Rocío/CSIC/University of Seville; Seville Spain

2. Centre for Biomedical Network Research on Rare Diseases (CIBERER); Seville Spain

3. Department of Pediatrics; University Hospital Virgen del Rocío; Seville Spain

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.37559/fullpdf

Reference16 articles.

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