Literature DB >> 3499643

[Weill-Marchesani syndrome].

J Herrera, M Morales.   

Abstract

Entities:  

Mesh：

Year:  1986        PMID： 3499643

Source DB:  PubMed          Journal:  Rev Chil Pediatr        ISSN： 0370-4106


× No keyword cloud information.
  2 in total

1.  Homozygous mutations in ADAMTS10 and ADAMTS17 cause lenticular myopia, ectopia lentis, glaucoma, spherophakia, and short stature.

Authors:  Jose Morales; Latifa Al-Sharif; Dania S Khalil; Jameela M A Shinwari; Prashant Bavi; Rahima A Al-Mahrouqi; Ali Al-Rajhi; Fowzan S Alkuraya; Brian F Meyer; Nada Al Tassan
Journal:  Am J Hum Genet       Date:  2009-11       Impact factor: 11.025

2.  Whole exome sequencing identifies a novel splice-site mutation in ADAMTS17 in an Indian family with Weill-Marchesani syndrome.

Authors:  Mohd Hussain Shah; Vishwanath Bhat; Jyoti S Shetty; Arun Kumar
Journal:  Mol Vis       Date:  2014-06-12       Impact factor: 2.367
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.