Molecular genetic analysis of the 17p11.2 region in patients with hereditary neuropathy with liability to pressure palsies (HNPP)

Human Genetics

Volumn 97, Issue 1, 1996, Pages 26-34

  Timmerman, Vincent ^a   Löfgren, Ann ^a   Le Guern, Eric ^b   Liang, Ping ^a   De Jonghe, Peter ^a,c   Martin, Jean Jacques ^a,c   Verhalle, Damienne ^d   Robberecht, Wim ^d   Gouider, Riadh ^b   Brice, Alexis ^b   Van Broeckhoven, Christine ^a  

^a UNIVERSITY OF ANTWERP   (Belgium)

^b PITIÉ SALPÊTRIÈRE HOSPITAL   (France)

^c ANTWERP UNIVERSITY HOSPITAL   (Belgium)

^d UNIVERSITY HOSPITALS LEUVEN   (Belgium)

Author keywords

[No Author keywords available]

Indexed keywords

DNA MARKER;

ARTICLE; BELGIUM; CHROMOSOME 17P; CLINICAL ARTICLE; CROSSING OVER; FRANCE; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; HUMAN CELL; INTERSTITIAL CHROMOSOME DELETION; MOLECULAR GENETICS; NEUROPATHY; PARALYSIS; PRIORITY JOURNAL; PULSED FIELD GEL ELECTROPHORESIS; TANDEM REPEAT;

EID: 13344260003     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/BF00218828     Document Type: Article

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