Charcot-Marie-Tooth disease type 1A: the parental origin of a de novo 17p11.2-p12 duplication-Reference-Cited by-同舟云学术

Charcot-Marie-Tooth disease type 1A: the parental origin of a de novo 17p11.2-p12 duplication

Published:2008-06-28 Issue:4 Volume:46 Page:291-294
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:

Author:

Hertz Jens Michael,Børglum Anders D.,Brandt Carsten A.,Flint Tracey,Bisgaard Carsten

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1994.tb04162.x/fullpdf

Reference22 articles.

1. Char-cot-Marie-Tooth (CMT) la duplication at 17p11.2 in Italian families;Bellone;J Med Genet,1992

2. Linkage localization of X-linked Char-cot-Marie-Tooth disease;Bergoffen;Am J Hum Genet,1993

3. Genetic linkage and heterogeneity in type I Charcot-Marie-Tooth disease (hereditary motor and sensory neuropathy type I);Chance;Am J Hum Genet,1990

4. Analysis of the DNA duplication 17p11.2 in Charcot-Marie-Tooth neuropathy type 1 pedigrees: additional evidence for a third autosomal CMT1 locus;Chance;Neurology,1992

5. Lower motor and primary sensory neuron diseases with peroneal muscular atrophy. I. Neurologic, genetic, and electrophysiologic findings in hereditary polyneuropathies;Dyck;Arch Neurol,1968

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