Localization of the gene for Wieacker-Wolff syndrome in the pericentromeric region of the X chromosome-Reference-Cited by-同舟云学术

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Localization of the gene for Wieacker-Wolff syndrome in the pericentromeric region of the X chromosome

Published:1997-08-04 Issue:3-4 Volume:100 Page:426-430
ISSN:0340-6717
Container-title:Human Genetics
language:
Short-container-title:Human Genetics

Author:

Kloos D.-U.,Jakubiczka S.,Wienker T.,Wolff G.,Wieacker P.

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/s004390050528.pdf

Cited by 15 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. Optic nerve abnormalities in female-restricted Wieacker-Wolff syndrome by a novel variant in the ZC4H2 gene;Ophthalmic Genetics;2023-07-31

2. Variable Phenotypes of ZC4H2-Associated Rare Disease in Six Patients;Annals of Child Neurology;2022-07-01

3. A novel de novo nonsense mutation in ZC4H2 causes Wieacker‐Wolff Syndrome;Molecular Genetics & Genomic Medicine;2019-12-30

4. Rnf220 cooperates with Zc4h2 to specify spinal progenitor domains;Development;2018-09-01

5. Wieacker-Wolff syndrome with associated cleft palate in a female case;American Journal of Medical Genetics Part A;2017-11-17

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