Crossover analysis in a British family suggests that Coffin-Lowry syndrome maps to a 3.4-cM interval in Xp22-Reference-Cited by-同舟云学术

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Crossover analysis in a British family suggests that Coffin-Lowry syndrome maps to a 3.4-cM interval in Xp22

Published:1995-12-04 Issue:4 Volume:59 Page:512-516
ISSN:0148-7299
Container-title:American Journal of Medical Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Bird Helen,Collins Amanda L.,Oley Christine,Lindsay Susan

Publisher

Wiley

Subject

Genetics(clinical)

Reference23 articles.

1. A 6-Mb YAC contig in Xp22.1–p22.2 spanning the DXS69E, XE59, GLRA2, PIGA, GRPR, CALB3, and PHKA2 genes

2. ABNORMAL PROTEODERMATAN SULFATE IN THREE PATIENTS WITH COFFIN-LOWRY SYNDROME

3. Construction of a High-Resolution Linkage Map for Xp22.1-p22.2 and Refinement of the Genetic Localization of the Coffin-Lowry Syndrome Gene

4. Dinucleotide repeat polymorphisms at the DXS365, DXS443 and DXS451 loci

Cited by 11 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. Hereditary Diseases That Implicate Defective Responses to DNA Damage;DNA Repair and Mutagenesis;2014-04-30

2. Postmortem findings in the Coffin-Lowry Syndrome;Genetics in Medicine;2003-05

3. Cognitive function in Coffin-Lowry syndrome;Clinical Genetics;2002-04

4. Genetic effects on human cognition: lessons from the study of mental retardation syndromes;Journal of Neurology, Neurosurgery & Psychiatry;2002-03-01

5. RSK2 represses HSF1 activation during heat shock;Cell Stress & Chaperones;2000

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