Localization of a Gene for Duane Retraction Syndrome to Chromosome 2q31-Reference-Cited by-同舟云学术

Localization of a Gene for Duane Retraction Syndrome to Chromosome 2q31

Published:1999-12 Issue:6 Volume:65 Page:1639-1646
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Appukuttan Binoy,Gillanders Elizabeth,Juo Suh-Hang,Freas-Lutz Diana,Ott Sandra,Sood Raman,Van Auken Ann,Bailey-Wilson Joan,Wang Xiaoguang,Patel Reshma J.,Robbins Christiane M.,Chung Mina,Annett Geralyn,Weinberg Kenneth,Borchert Mark S.,Trent Jeffrey M.,Brownstein Michael J.,Stout J. Timothy

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference39 articles.

1. Analysis of the Hoxd-3 gene: structure and localization of its sense and natural antisense transcripts;Bedford;DNA Cell Biol,1995

2. Detection of an insertion deletion of region 8q13-q21.2 in a patient with Duane syndrome: implications for mapping and cloning a Duane gene;Calabrese;Eur J Hum Genet,1998

3. Loss of Hox-A1 (Hox-1.6) function results in the reorganization of the murine hindbrain;Carpenter;Development,1993

4. Duane's retraction syndrome associated with chromosome 4q27-31 segment deletion;Chew;Am J Ophthalmol,1995

5. Chung M, Stout JT, Borchert MS. Clinical diversity of hereditary duane's retraction syndrome. Ophthalmology (in press)

Cited by 95 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. Relationship between retraction and refraction values in patients with Duane's retraction syndrome;Journal Français d'Ophtalmologie;2024-09

2. Identifying novel disease genes and revealing the pathomechanism of monogenic diseases;Pediatrics International;2024-01

3. Two novel CHN1 variants identified in Duane retraction syndrome pedigrees disrupt development of ocular motor nerves in zebrafish;Journal of Human Genetics;2023-10-18

4. DUANE SYNDROME:;Health and Society;2023-05-05

5. A Chinese family with cat eye syndrome and abnormality of eye movement: First case report;Frontiers in Pediatrics;2023-04-11