Homozygosity mapping of a Weill-Marchesani syndrome locus to chromosome 19p13.3-p13.2-Reference-Cited by-同舟云学术

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Homozygosity mapping of a Weill-Marchesani syndrome locus to chromosome 19p13.3-p13.2

Published:2002-03-13 Issue:4 Volume:110 Page:366-370
ISSN:0340-6717
Container-title:Human Genetics
language:en
Short-container-title:Hum Genet

Author:

Faivre Laurence,Mégarbané André,Alswaid Abdulrahman,Zylberberg Louise,Aldohayan Noura,Campos-Xavier Ana,Bacq Delphine,Legeai-Mallet Laurence,Bonaventure Jacky,Munnich Arnold,Cormier-Daire Valérie

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/s00439-002-0689-3.pdf

Cited by 39 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. Congenital anomalies of lens shape;TAIWAN J OPHTHALMOL;2023

2. Characteristics and genotype–phenotype correlations in ADAMTS17 mutation–related Weill–Marchesani syndrome;Experimental Eye Research;2023-09

3. TGF-β and BMP Signaling Pathways in Skeletal Dysplasia with Short and Tall Stature;Annual Review of Genomics and Human Genetics;2023-08-25

4. A Novel Mutation in the ADAMTS10 Associated with Weil–Marchesani Syndrome with a Unique Presentation of Developed Membranes Causing Severe Stenosis of the Supra Pulmonic, Supramitral, and Subaortic Areas in the Heart;International Journal of Molecular Sciences;2023-05-16

5. Congenital anomalies of lens shape;Taiwan Journal of Ophthalmology;2023

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