Hereditary neuralgic amyotrophy

Current Opinion in Neurology

Volumn 9, Issue 5, 1996, Pages 343-347

  Chance, Phillip F ^a,b   Windebank, Anthony J ^c  

^a CHILDREN S HOSPITAL OF PHILADELPHIA   (United States)

^b UNIVERSITY OF PENNSYLVANIA   (United States)

^c MAYO CLINIC   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DNA MARKER;

AUTOSOMAL DOMINANT DISORDER; BRACHIAL PLEXUS; CHROMOSOME 17P; CHROMOSOME 17Q; CLINICAL FEATURE; FACE DYSMORPHIA; GENE MAPPING; GENETIC LINKAGE; HUMAN; HYPOTELORISM; MOLECULAR BIOLOGY; MUSCLE ATROPHY; NEURALGIA; NEUROPATHY; NOSE; PARALYSIS; POLYMERASE CHAIN REACTION; SHORT SURVEY;

EID: 0029905967     PISSN: 13507540     EISSN: None     Source Type: Journal    
DOI: 10.1097/00019052-199610000-00005     Document Type: Short Survey

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