A further case of Skraban-Deardorff syndrome and review of the literature-Reference-Cited by-同舟云学术

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A further case of Skraban-Deardorff syndrome and review of the literature

Published:2021-11-12 Issue: Volume:Publish Ahead of Print Page:
ISSN:0962-8827
Container-title:Clinical Dysmorphology
language:en
Short-container-title:

Author:

Shirley Cheng Sze Wing,Luk Ho-Ming,Lo Fai Man Ivan

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Genetics (clinical),General Medicine,Pathology and Forensic Medicine,Anatomy,Pediatrics, Perinatology and Child Health

Cited by 3 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. Skraban‐Deardorff intellectual disability syndrome‐associated mutations in WDR26 impair CTLH E3 complex assembly;FEBS Letters;2024-04-04

2. Skraban-Deardorff Syndrome in an Indian Child - A Very Rare Pathogenic Base Pair Deletion in WDR26 Gene;Indian Journal of Pediatrics;2023-12-06

3. New clinical features in an adult patient with Skraban‐Deardorff syndrome;American Journal of Medical Genetics Part A;2022-10-21

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