First report of two successive deletions on chromosome 15q13 cytogenetic bands in a boy and girl: additional data to 15q13.3 syndrome with a report of high IQ patient-Reference-Cited by-同舟云学术

First report of two successive deletions on chromosome 15q13 cytogenetic bands in a boy and girl: additional data to 15q13.3 syndrome with a report of high IQ patient

Published:2019-05-18 Issue:1 Volume:12 Page:
ISSN:1755-8166
Container-title:Molecular Cytogenetics
language:en
Short-container-title:Mol Cytogenet

Author:

Alsagob Maysoon,Salih Mustafa A.,Hamad Muddathir H. A.,Al-Yafee Yusra,Al-Zahrani Jawaher,Al-Bakheet Albandary,Nester Michael,Sakati Nadia,Wakil Salma M.,AlOdaib Ali,Colak Dilek,Kaya Namik^ORCID

Funder

King Salman Center for Disability Research

King Abdulaziz City for Science and Technology

Deanship of Scientific Research, King Saud University

Publisher

Springer Science and Business Media LLC

Subject

Biochemistry, medical,Genetics(clinical),Genetics,Molecular Biology,Molecular Medicine,Biochemistry

Link

http://link.springer.com/content/pdf/10.1186/s13039-019-0432-6.pdf

Reference38 articles.

1. Sharp AJ, Mefford HC, Li K, Baker C, Skinner C, Stevenson RE, Schroer RJ, Novara F, De Gregori M, Ciccone R, et al. A recurrent 15q13.3 microdeletion syndrome associated with mental retardation and seizures. Nat Genet. 2008;40(3):322–8.