Linkage in a family with X-linked Charcot-Marie-Tooth disease
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1989.tb02964.x/fullpdf
Reference17 articles.
1. Localization of X-linked dominant Charcot-Marie-Tooth disease (CMT2) to Xq13;Beckett;J. Neurogenet.,1986
2. A technique for radiolabelling DNA restriction endonuclease fragments to high specific activity;Feinberg;Anal. Biochem.,1983
3. Findlay , J. 1935 Neural Progressive Muscular Atrophy: A Study in Heredity. Thesis
4. X-linked neuropathy: gene localisation with DNA probes;Fischbeck;Ann. Neurol.,1986
5. X-linked dominant Charcot-Marie-Tooth disease: suggestion of linkage with a cloned DNA sequence from the proximal Xq;Gal;Hum. Genet.,1985
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2. Hereditary motor and sensory neuropathy type I, associated with aplasia cutis congenital possible X-linked inheritance;Clinical Genetics;2008-06-28
3. Molecular genetics of X-linked Charcot-Marie-Tooth disease;NeuroMolecular Medicine;2006-03
4. Julia Bell and the Treasury of Human Inheritance;Human Genetics;2005-02-26
5. X-linked Charcot-Marie-Tooth Disease;Peripheral Neuropathy;2005
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