A novel mutation in the IHH gene causes brachydactyly type A1: a 95-year-old mystery resolved-Reference-Cited by-同舟云学术

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A novel mutation in the IHH gene causes brachydactyly type A1: a 95-year-old mystery resolved

Published:2002-10-01 Issue:4-5 Volume:111 Page:368-375
ISSN:0340-6717
Container-title:Human Genetics
language:
Short-container-title:Human Genetics

Author:

McCready Elizabeth,Sweeney Elizabeth,Fryer Allan,Donnai Dian,Baig Akeel,Racacho Lemuel,Warman Matthew,Hunter Alasdair,Bulman Dennis

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/s00439-002-0815-2.pdf

Cited by 42 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. Suppression of apoptosis impairs phalangeal joint formation in the pathogenesis of brachydactyly type A1;Nature Communications;2024-03-12

2. Novel PTCH1 Mutation Causes Gorlin-Goltz Syndrome;CHIN J DENT RES;2024

3. Deletion of 2 amino acids in IHH in a Japanese family with brachydactyly type A1;BMC Medical Genomics;2021-07-27

4. A novel variant of IHH in a Chinese family with brachydactyly type 1;BMC Medical Genetics;2020-03-24

5. Whole-exome sequencing identifies a novel IHH insertion in an Ontario family with brachydactyly type A1;SAGE Open Medical Case Reports;2018-01

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