Functional Null Mutations in the Gonosomal Homologue Gene TBL1Y are Associated with Non-Syndromic Coarctation of the Aorta-Reference-Cited by-同舟云学术

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Functional Null Mutations in the Gonosomal Homologue Gene TBL1Y are Associated with Non-Syndromic Coarctation of the Aorta

Published:2012-02-01 Issue:2 Volume:12 Page:199-205
ISSN:1566-5240
Container-title:Current Molecular Medicine
language:en
Short-container-title:CMM

Author:

Tagariello A.,Breuer C.,Birkner Y.,Schmidt S.,Koch A.M.,Cesnjevar R.,Ruffer A.,Dittrich S.,Schneider H.,Winterpacht A.,Sticht H.,Dotsch J.,Toka O.

Publisher

Bentham Science Publishers Ltd.

Subject

Molecular Biology,Molecular Medicine,General Medicine,Biochemistry

Cited by 18 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. Embryonic expression patterns of TBL1 family in zebrafish;Gene Expression Patterns;2024-03

2. Human Genetics of Congenital Heart Defects;Advances in Experimental Medicine and Biology;2024

3. The Advent of Spatial Omics in Congenital Heart Disease;Current Treatment Options in Pediatrics;2023-11-08

4. Isolated Coarctation of the Aorta: Current Concepts and Perspectives;Frontiers in Cardiovascular Medicine;2022-05-25

5. Y chromosome is moving out of sex determination shadow;Cell & Bioscience;2022-01-04

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