Novel mutations in the gene SALL4 provide further evidence for acro-renal-ocular and Okihiro syndromes being allelic entities, and extend the phenotypic spectrum-Reference-Cited by-同舟云学术

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Novel mutations in the gene SALL4 provide further evidence for acro-renal-ocular and Okihiro syndromes being allelic entities, and extend the phenotypic spectrum

Published:2004-08-01 Issue:8 Volume:41 Page:e102-e102
ISSN:1468-6244
Container-title:Journal of Medical Genetics
language:en
Short-container-title:Journal of Medical Genetics

Author:

Borozdin W

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Cited by 58 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. SALL4 deletion and kidney and cardiac defects associated with VACTERL association;Pediatric Nephrology;2024-02-08

2. SALL4 deletion and renal and cardiac defects associated with VACTERL association;2024-01-02

3. Human Genetics of Tetralogy of Fallot and Double-Outlet Right Ventricle;Advances in Experimental Medicine and Biology;2024

4. Structure of SALL4 zinc finger domain reveals link between AT-rich DNA binding and Okihiro syndrome;Life Science Alliance;2023-01-12

5. Structural analysis of SALL4 zinc-finger domain reveals a link between AT-rich DNA binding and Okihiro syndrome;2022-06-14

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