Multimodal imaging of retinal findings in syndactyly, telecanthus, anogenital, and renal malformations (STAR) syndrome-Reference-Cited by-同舟云学术

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Multimodal imaging of retinal findings in syndactyly, telecanthus, anogenital, and renal malformations (STAR) syndrome

Published:2022-03 Issue: Volume:25 Page:101284
ISSN:2451-9936
Container-title:American Journal of Ophthalmology Case Reports
language:en
Short-container-title:American Journal of Ophthalmology Case Reports

Author:

Li Alexa L.^ORCID,Borooah Shyamanga,Nudleman Eric

Publisher

Elsevier BV

Subject

Ophthalmology

Reference11 articles.

1. Mutations in the cyclin family member FAM58A cause an X-linked dominant disorder characterized by syndactyly, telecanthus and anogenital and renal malformations;Unger;Nat Genet,2008

2. STAR syndrome-associated CDK10/Cyclin M regulates actin network architecture and ciliogenesis;Guen;Cell Cycle,2016

3. STAR syndrome: a further case and the first report of maternal mosaicism;Lefroy;Clin Dysmorphol,2017

4. STAR syndrome plus: the first description of a female patient with the lethal form;Bedeschi;Am J Med Genet,2017

5. Multigenerational pedigree with STAR syndrome: a novel FAM58A variant and expansion of the phenotype;Boczek;Am J Med Genet,2017

Cited by 1 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. Novel mutation in the SALL1 gene in a four-generation Chinese family with uraemia: A case report;World Journal of Clinical Cases;2022-07-16

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