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American Journal of Medical Genetics, Part A

Volumn 152, Issue 2, 2010, Pages 484-485

Mowat-Wilson syndrome with associated dysphagia

(2) Prijoles, Eloise J a Adam, Margaret b

a UNIVERSITY OF SOUTH FLORIDA (United States)

b EMORY UNIVERSITY SCHOOL OF MEDICINE (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ANAMNESIS; AUTOSOMAL DOMINANT DISORDER; CASE REPORT; CHILD; CLINICAL FEATURE; CRANIOFACIAL MALFORMATION; DEVELOPMENTAL DISORDER; DISEASE ASSOCIATION; DYSPHAGIA; FEEDING DISORDER; FEMALE; GENE; GENE MUTATION; HUMAN; HYPERTELORISM; LETTER; MALE; MICROCEPHALY; MOWAT WILSON SYNDROME; MUSCLE HYPOTONIA; NUCLEAR MAGNETIC RESONANCE IMAGING; PRESCHOOL CHILD; PRIORITY JOURNAL; SCHOOL CHILD; SYNDACTYLY; UNDERWEIGHT; ZEB2 GENE;

ABNORMALITIES, MULTIPLE; CHILD; CHILD, PRESCHOOL; CORPUS CALLOSUM; CRANIOFACIAL ABNORMALITIES; DEGLUTITION DISORDERS; FEMALE; GASTROINTESTINAL TRACT; HEART DEFECTS, CONGENITAL; HOMEODOMAIN PROTEINS; HUMANS; MAGNETIC RESONANCE IMAGING; MALE; REPRESSOR PROTEINS; SYNDROME; UROGENITAL ABNORMALITIES;

EID: 75449117085 PISSN: 15524825 EISSN: 15524833 Source Type: Journal
DOI: 10.1002/ajmg.a.33211 Document Type: Letter

Times cited : (2)

References (5)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.