Estimation of the size of the chromosome 17p11.2 duplication in Charcot-Marie-Tooth neuropathy type 1a (CMT1a). HMSN Collaborative Research Group.

Author:

Raeymaekers P,Timmerman V,Nelis E,Van Hul W,De Jonghe P,Martin J J,Van Broeckhoven C

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference28 articles.

1. Inherited neuronal degeneration and atrophy affecting peripheral motor, sensory, and autonomic neurons;Dyck, P.J.,1984

2. The nosology of genetic peripheral neuropathies in Swedish children;Hagberg, B.; Westerberg, B.;Acta Paediatr Scand,1983

3. Prevalence of hereditary motor and sensory neuropathy in Cantabria;Acta Neurol Scand,1987

4. Genetic aspects of hereditary motor and sensory neuropathy (type I and II);Harding, A.E.; Thomas, P.K.;J Med Genet,1980

5. Linkage of dominantly inherited Charcot-Marie-Tooth neuropathy to the Duffy locus in an Indiana family;Stebbins, N.B.; Conneally, P.M.;Am J Hum Genet; Genetic linkage of hereditary motor and sensory neuropathy type I (Charcot-MarieTooth disease) to markers of chromosomes 1 and 17,1982

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