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期刊界 All Journals 搜尽天下杂志传播学术成果专业期刊搜索期刊信息化学术搜索

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

Authors:	Raquel M. Fernández Javier Sánchez Lutgardo García‐Díaz Yolanda Peláez‐Nora Antonio González‐Meneses Guillermo Antiñolo Salud Borrego

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;4. Correspondence to:;5. Salud Borrego, M.D., Ph.D., Department of Genetics, Reproduction and Fetal Medicine, University Hospital Virgen del Rocío, Av Manuel Siurot s/n, Seville 41013, Spain.;6. E‐mail:

Abstract:

Keywords:	interstitial insertion 10p monosomy familial 10p deletion DiGeorge syndrome type 2 HDR syndrome