Recombination hot spot in a 3.2-kb region of the Charcot-Marie-Tooth type 1A repeat sequences: new tools for molecular diagnosis of hereditary neuropathy with liability to pressure palsies and of Charcot-Marie-Tooth type 1A. French CMT Collaborative Research Group.

Lopes, J; LeGuern, E; Gouider, R; Tardieu, S; Abbas, N; Birouk, N; Gugenheim, M; Bouche, P; Agid, Y; Brice, A

Lopes, J; LeGuern, E; Gouider, R; Tardieu, S; Abbas, N; Birouk, N; Gugenheim, M; Bouche, P; Agid, Y; Brice, A.

Affiliation

Lopes J; INSERM U289, Hôpital de la Salpêtrière, Paris, France.

Am J Hum Genet ; 58(6): 1223-30, 1996 Jun.

Article in En | MEDLINE | ID: mdl-8651299

Subject(s)

Charcot-Marie-Tooth Disease/genetics; Chromosomes, Human, Pair 17; Hereditary Sensory and Motor Neuropathy/genetics; Recombination, Genetic; Repetitive Sequences, Nucleic Acid; Charcot-Marie-Tooth Disease/classification; Charcot-Marie-Tooth Disease/diagnosis; Chromosome Mapping; Chromosomes, Artificial, Yeast; Cloning, Molecular; Crossing Over, Genetic; Genomic Library; Genotype; Hereditary Sensory and Motor Neuropathy/classification; Hereditary Sensory and Motor Neuropathy/diagnosis; Humans; Polymorphism, Genetic; Restriction Mapping

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Recombination, Genetic / Chromosomes, Human, Pair 17 / Repetitive Sequences, Nucleic Acid / Hereditary Sensory and Motor Neuropathy / Charcot-Marie-Tooth Disease Type of study: Clinical_trials / Diagnostic_studies Limits: Humans Language: En Journal: Am J Hum Genet Year: 1996 Document type: Article Affiliation country: France Country of publication: United States

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