Targeted exome sequencing reveals a novel GLI3 mutation in a Chinese family with nonsyndromic polydactyly-Reference-Cited by-同舟云学术

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Targeted exome sequencing reveals a novel GLI3 mutation in a Chinese family with nonsyndromic polydactyly

Published:2019-07-24 Issue:10 Volume:248 Page:942-947
ISSN:1058-8388
Container-title:Developmental Dynamics
language:en
Short-container-title:Developmental Dynamics

Author:

Zhao Xiangyu¹^ORCID,Xu Hongyan¹,Liu Xiaxia¹,Li Lin¹

Affiliation:

1. Department of Medical GeneticsLinyi People's Hospital Linyi Shandong Province China

Funder

Natural Science Foundation of Shandong Province

Publisher

Wiley

Subject

Developmental Biology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/dvdy.89

Reference18 articles.

1. GLI3-related polydactyly: a review

2. Polydactyly: phenotypes, genetics and classification

3. Common congenital hand conditions;Chong AK;Singapore Med J,2010

4. Clinical and descriptive genetic study of polydactyly: a Pakistani experience of 313 cases

5. Polydactyly: How many disorders and how many genes? 2010 update

Cited by 2 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. All-trans-retinoic acid suppresses rat embryo hindlimb bud mesenchymal chondrogenesis by modulating HoxD9 expression;Bioengineered;2021-01-01

2. Novel frameshift mutations of ANKUB1, GLI3, and TAS2R3 associated with polysyndactyly in a Chinese family;Molecular Genetics & Genomic Medicine;2020-04-06

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