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

American Journal of Human Genetics

Volumn 58, Issue 6, 1996, Pages 1223-1230

  Lopes, J ^a   LeGuern, E ^a   Gouider, R ^a   Tardieu, S ^a   Abbas, N ^a   Birouk, N ^a   Gugenheim, M ^a   Bouche, P ^a   Agid, Y ^a   Brice, A ^a   Arne Bes, M C ^a   Brichet, B ^a   Chapon, F ^a   Chazot, G ^a   Clavelou, P ^a   Desnuelle, C ^a   Diraison, P ^a   Dubas, F ^a   Gonnaud, P M ^a  

^a PITIÉ SALPÊTRIÈRE HOSPITAL   (France)

Author keywords

[No Author keywords available]

Indexed keywords

DNA;

ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CHROMOSOME 17P; CROSSING OVER; DIAGNOSTIC TEST; FAMILY STUDY; GENE MAPPING; GENE REARRANGEMENT; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; HUMAN CELL; MAJOR CLINICAL STUDY; NUCLEOTIDE REPEAT; NUCLEOTIDE SEQUENCE; PERIPHERAL NEUROPATHY; PRIORITY JOURNAL; SEQUENCE HOMOLOGY; SOUTHERN BLOTTING;

CHARCOT-MARIE-TOOTH DISEASE; CHROMOSOME MAPPING; CHROMOSOMES, ARTIFICIAL, YEAST; CHROMOSOMES, HUMAN, PAIR 17; CLONING, MOLECULAR; CROSSING OVER, GENETIC; GENOMIC LIBRARY; GENOTYPE; HEREDITARY MOTOR AND SENSORY NEUROPATHIES; HUMANS; POLYMORPHISM, GENETIC; RECOMBINATION, GENETIC; REPETITIVE SEQUENCES, NUCLEIC ACID; RESTRICTION MAPPING;

EID: 0029989649     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (0)