Cockayne syndrome in three sisters with varying clinical presentation-Reference-Cited by-同舟云学术

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Cockayne syndrome in three sisters with varying clinical presentation

Published:2002-07-15 Issue:1 Volume:111 Page:81-85
ISSN:0148-7299
Container-title:American Journal of Medical Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Mahmoud Adel A.H.,Yousef George M.,Al-Hifzi Ibrahim,Diamandis Eleftherios P.

Publisher

Wiley

Subject

Genetics(clinical)

Reference28 articles.

1. Prenatal diagnosis of xeroderma pigmentosum and cockayne syndrome

2. Dwarfism with retinal atrophy and deafness

3. Dwarfism with Retinal Atrophy and Deafness

4. Defective Transcription-Coupled Repair of Oxidative Base Damage in Cockayne Syndrome Patients from XP Group G

Cited by 15 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. Very early prenatal diagnosis of Cockayne’s syndrome by coelocentesis;Journal of Obstetrics and Gynaecology;2022-01-10

2. Genetic Abnormalities of the Retina and Choroid;Ophthalmic Genetic Diseases;2019

3. Allelic interaction effects of DNA damage and repair genes on the predisposition to age-related cataract;PLOS ONE;2018-04-24

4. Photosensitivity and Photoreactions;Hurwitz Clinical Pediatric Dermatology;2016

5. A new mutation in the CSB gene in a C hinese patient with mild C ockayne syndrome;Clinical Case Reports;2014-02-07

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