Craniofacial and cutaneous findings expand the phenotype of hereditary neuralgic amyotrophy

Neurology

Volumn 57, Issue 11, 2001, Pages 1963-1968

  Jeannet, Pierre Yves ^a   Watts, Giles D J ^b   Bird, Thomas D ^b,c   Chance, Phillip F ^a,b  

^a SEATTLE CHILDREN S RESEARCH INSTITUTE   (United States)

^b UNIVERSITY OF WASHINGTON SCHOOL OF MEDICINE   (United States)

^c VA Puget Sound Medical Center   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; AUTOSOMAL DOMINANT DISORDER; BRACHIAL PLEXUS NEUROPATHY; CHILD; CHROMOSOME 17Q; CLEFT PALATE; CLINICAL ARTICLE; CONTROLLED STUDY; CRANIOFACIAL MORPHOLOGY; DISEASE COURSE; FEMALE; HUMAN; HYPOTELORISM; MALE; PHENOTYPE; PRIORITY JOURNAL; SKINFOLD;

EID: 0035846539     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/WNL.57.11.1963     Document Type: Article

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