BMPR1A is a candidate gene for congenital heart defects associated with the recurrent 10q22q23 deletion syndrome-Reference-Cited by-同舟云学术

BMPR1A is a candidate gene for congenital heart defects associated with the recurrent 10q22q23 deletion syndrome

Published:2012-01 Issue:1 Volume:55 Page:12-16
ISSN:1769-7212
Container-title:European Journal of Medical Genetics
language:en
Short-container-title:European Journal of Medical Genetics

Author:

Breckpot Jeroen,Tranchevent Léon-Charles,Thienpont Bernard,Bauters Marijke,Troost Els,Gewillig Marc,Vermeesch Joris R.,Moreau Yves,Devriendt Koenraad,Van Esch Hilde

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics,General Medicine

Reference29 articles.

1. Recurrent 10q22-q23 deletions: a genomic disorder on 10q associated with cognitive and behavioral abnormalities;Balciuniene;American Journal of Human Genetics,2007

2. Clinical and molecular characterization of individuals with recurrent genomic disorder at 10q22.3q23.2;Alliman;Clinical Genetics,2010

3. The phenotype of recurrent 10q22q23 deletions and duplications;van Bon;European Journal of Human Genetics: EJHG,2011

4. Variable phenotypes associated with 10q23 microdeletions involving the PTEN and BMPR1A genes;Menko;Clinical Genetics,2008

5. Contiguous gene deletion within chromosome arm 10q is associated with juvenile polyposis of infancy, reflecting cooperation between the BMPR1A and PTEN tumor-suppressor genes;Delnatte;American Journal of Human Genetics,2006

Cited by 25 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. Effect of genetic profiling on surgical decisions at hereditary colorectal cancer syndromes;Heliyon;2024-08

2. A critical review of the impact of candidate copy number variants on autism spectrum disorder;Mutation Research - Reviews in Mutation Research;2024-07

3. Thiram exposure induces tibial dyschondroplasia in broilers via the regulation effect of circ_003084/miR-130c-5p/BMPR1A crosstalk on chondrocyte proliferation and differentiation;Journal of Hazardous Materials;2024-03

4. Genotype–phenotype correlation of BMPR1a disease causing variants in juvenile polyposis syndrome;Hereditary Cancer in Clinical Practice;2023-07-03

5. Systems analysis of de novo mutations in congenital heart diseases identified a protein network in the hypoplastic left heart syndrome;Cell Systems;2022-11