Literature DB >> 8702121

Progress in human chondrodysplasias: molecular genetics.

W A Horton1.   

Abstract

Entities:  

Mesh:

Substances:

Year:  1996        PMID: 8702121     DOI: 10.1111/j.1749-6632.1996.tb56253.x

Source DB:  PubMed          Journal:  Ann N Y Acad Sci        ISSN: 0077-8923            Impact factor:   5.691


× No keyword cloud information.
  2 in total

Review 1.  Clinical and Molecular genetics of Stickler syndrome.

Authors:  M P Snead; J R Yates
Journal:  J Med Genet       Date:  1999-05       Impact factor: 6.318

2.  COL2A1 exon 2 mutations: relevance to the Stickler and Wagner syndromes.

Authors:  A J Richards; S Martin; J R Yates; J D Scott; D M Baguley; F M Pope; M P Snead
Journal:  Br J Ophthalmol       Date:  2000-04       Impact factor: 4.638

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.