Literature DB >> 13709149

A family study of aniridia.

J H GROVE, M W SHAW, G BOURQUE.   

Abstract

Entities:  

Keywords:  IRIS/abnormalities

Mesh：

Year:  1961        PMID： 13709149     DOI： 10.1001/archopht.1961.01840020083016

Source DB:  PubMed          Journal:  Arch Ophthalmol        ISSN： 0003-9950


× No keyword cloud information.
  4 in total

1.  Congenital aniridia: long-term clinical course, visual outcome, and prognostic factors.

Authors:  Ji Woong Chang; Jeong Hun Kim; Seong-Joon Kim; Young Suk Yu
Journal:  Korean J Ophthalmol       Date:  2014-11-19

2.  A probable case of the homozygous condition of the aniridia gene.

Authors:  S V Hodgson; K E Saunders
Journal:  J Med Genet       Date:  1980-12       Impact factor: 6.318

3.  Autosomal dominant aniridia: probable linkage to acid phosphatase-1 locus on chromosome 2.

Authors:  R E Ferrell; A Chakravarti; H M Hittner; V M Riccardi
Journal:  Proc Natl Acad Sci U S A       Date:  1980-03       Impact factor: 11.205

4.  Molecular analysis of the PAX6 gene in Mexican patients with congenital aniridia: report of four novel mutations.

Authors:  Camilo E Villarroel; Cristina Villanueva-Mendoza; Lorena Orozco; Miguel Angel Alcántara-Ortigoza; Diana F Jiménez; Juan C Ordaz; Ariadna González-del Angel
Journal:  Mol Vis       Date:  2008-09-08       Impact factor: 2.367
  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.