Literature DB >> 11132670

Posterior microphthalmos associated with papillomacular fold and high hyperopia.

D Goldblum1, D S Mojon.   

Abstract

Entities:  

Mesh：

Year:  1999        PMID： 11132670     DOI： 10.3928/0191-3913-19991101-13

Source DB:  PubMed          Journal:  J Pediatr Ophthalmol Strabismus        ISSN： 0191-3913            Impact factor:   1.402


× No keyword cloud information.
  3 in total

1.  A genome-wide linkage scan in Tunisian families identifies a novel locus for non-syndromic posterior microphthalmia to chromosome 2q37.1.

Authors:  Mounira Hmani-Aifa; Salma Ben Salem; Zeineb Benzina; Walid Bouassida; Riadh Messaoud; Khalil Turki; Moncef Khairallah; Ahmed Rebaï; Faïza Fakhfekh; Peter Söderkvist; Hammadi Ayadi
Journal:  Hum Genet       Date:  2009-06-14       Impact factor: 4.132

2.  Novel truncation mutations in MYRF cause autosomal dominant high hyperopia mapped to 11p12-q13.3.

Authors:  Xueshan Xiao; Wenmin Sun; Jiamin Ouyang; Shiqiang Li; Xiaoyun Jia; Zhiqun Tan; J Fielding Hejtmancik; Qingjiong Zhang
Journal:  Hum Genet       Date:  2019-06-06       Impact factor: 4.132

3.  Membrane frizzled-related protein gene-related ophthalmological syndrome: 30-month follow-up of a sporadic case and review of genotype-phenotype correlation in the literature.

Authors:  Alberto Neri; Rosachiara Leaci; Juan C Zenteno; Cristina Casubolo; Elisabetta Delfini; Claudio Macaluso
Journal:  Mol Vis       Date:  2012-10-26       Impact factor: 2.367
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.