Case of 15q26-qter deletion associated with a Prader-Willi phenotype-Reference-Cited by-同舟云学术

Case of 15q26-qter deletion associated with a Prader-Willi phenotype

Published:2020-08 Issue:8 Volume:63 Page:103955
ISSN:1769-7212
Container-title:European Journal of Medical Genetics
language:en
Short-container-title:European Journal of Medical Genetics

Author:

Santos Jéssica Fernandes dos,Acosta Angelina Xavier,Scheibler Gabriela Gayer,Pitanga Paula Monique Leite,Alves Esmeralda Santos,Meira Joanna Goes Castro,Zanardo Évelin Aline,Kulikowski Leslie Domenici,Lima Renata Lúcia Leite Ferreira de,Carvalho Acácia Fernandes Lacerda de

Funder

National Council for Scientific and Technological Development

CNPq

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics,General Medicine

Reference56 articles.

1. Aspects of growth hormone and insulin-like growth factor-I related to neuroprotection, regeneration, and functional plasticity in the adult brain;Aberg;Sci. World J.,2006

2. Homozygosity mapping in 64 Syrian consanguineous families with non-specific intellectual disability reveals 11 novel loci and high heterogeneity. European journal of human genetics;Abou Jamra;EJHG (Eur. J. Hum. Genet.),2011

3. Chromosomal microarray analysis of functional Xq27-qter disomy and deletion 3p26.3 in a boy with Prader-Willi like features and hypotonia;Ben-Abdallah-Bouhjar;Eur. J. Med. Genet.,2012

4. Terminal deletion of chromosome 15q26.1: case report and brief literature review;Bhakta;J. Perinatol.,2005

5. Loss-of-function mutations in SIM1 contribute to obesity and Prader-Willi–like features;Bonnefond;J. Clin. Invest.,2013

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Identifying Genetic Etiology in Patients with Intellectual Disability: An Experience in Public Health Services in Northeastern Brazil;Journal of Pediatric Genetics;2022-11-14