A new X-linked syndrome with muscle atrophy, congenital contractures, and oculomotor apraxia-Reference-Cited by-同舟云学术

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A new X-linked syndrome with muscle atrophy, congenital contractures, and oculomotor apraxia

Published:1985-04 Issue:4 Volume:20 Page:597-606
ISSN:0148-7299
Container-title:American Journal of Medical Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Wieacker Peter,Wolff Gerhard,Wienker Thomas F.,Sauer Michael,Opitz John M.,Reynolds James F.

Publisher

Wiley

Subject

Genetics (clinical)

Reference23 articles.

1. Progressive Ophthalmoplegia in Kugelberg-Welander Disease

2. Arthrogryposis Multiplex Congenita as Part of an Inherited Symptom Complex: Two Case Reports and a Review of the Literature

3. (1935) On the peroneal type of progressive muscular atrophy. In: “Treasury of Human Inheritance.” Vol 4, part VI. London: Cambridge University Press, pp 1-64.

Cited by 45 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. Loss of ZC4H2, an Arthrogryposis Multiplex Congenita Associated Gene, Promotes Osteoclastogenesis in Mice;Genes;2024-08-28

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

3. Loss of Protein Function Causing Severe Phenotypes of Female-Restricted Wieacker Wolff Syndrome due to a Novel Nonsense Mutation in the ZC4H2 Gene;Genes;2022-08-29

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

5. Ophthalmic abnormalities in Wieacker-Wolff syndrome;Journal of American Association for Pediatric Ophthalmology and Strabismus;2022-04

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