Polymorphisms in the PMP-22 gene region (17p11.2-12) are crucial for simplified diagnosis of duplications/deletions

Human Genetics

Volumn 99, Issue 5, 1997, Pages 688-691

  Haupt, Andrea ^a   Schöls, Ludger ^b   Przuntek, Horst ^b   Epplen, Jörg T ^a  

^a RUHR UNIVERSITY BOCHUM   (Germany)

^b ST JOSEF HOSPITAL   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

MYELIN PROTEIN; REPETITIVE DNA; RESTRICTION ENDONUCLEASE;

ARTICLE; CHROMOSOME 17P; DELETION MUTANT; DNA FLANKING REGION; DNA RECOMBINATION; GENE DUPLICATION; GENETIC POLYMORPHISM; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; MAJOR CLINICAL STUDY; PARALYSIS; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SOUTHERN BLOTTING;

EID: 1842326763     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004390050431     Document Type: Article

References (18)

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