Exclusion of primary congenital glaucoma (buphthalmos) from two candidate regions of chromosome arm 6p and chromosome 11-Reference-Cited by-同舟云学术

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Exclusion of primary congenital glaucoma (buphthalmos) from two candidate regions of chromosome arm 6p and chromosome 11

Published:1996-01-22 Issue:3 Volume:61 Page:290-292
ISSN:0148-7299
Container-title:American Journal of Medical Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Akarsu A. Nurten,Turacli M. Erol,Aktan S. Gulderen,Hossain Altaf,Barsoum-Homsy Magda,Chevrette Line,Sayli B. Sitki,Sarfarazi Mansoor

Publisher

Wiley

Subject

Genetics(clinical)

Reference16 articles.

1. High resolution of a small pericentric inversion of chromosome 11.

2. Incidence and Prognosis of Childhood Glaucoma

3. Congenital Glaucoma and Other Ocular Abnormalities Associated With Pericentric Inversion of Chromosome 11

4. Integrated human genome–wide maps constructed using the CEPH reference panel

5. The 1993–94 Généthon human genetic linkage map

Cited by 4 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. Recent advances in molecular genetics of glaucomas;Human Molecular Genetics;1997-09-01

2. Identification of three different truncating mutations in cytochrome P4501B1 (CYP1B1) as the principal cause of primary congenital glaucoma (Buphthalmos) in families linked to the GLC3A locus on chromosome 2p21;Human Molecular Genetics;1997-04-01

3. A second locus (GLC3B) for primary congenital glaucoma (Buphthalmos) maps to the 1p36 region;Human Molecular Genetics;1996-08-01

4. Localization of a Locus (GLC1B) for Adult-Onset Primary Open Angle Glaucoma to the 2cen–q13 Region;Genomics;1996-08

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