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American Journal of Medical Genetics, Part A

Volumn 155, Issue 12, 2011, Pages 3060-3062

Ablepharon-Macrostomia syndrome-Extension of the phenotype

(6) Kallish, Staci a Mcdonald Mcginn, Donna M a,b van Haelst, Mieke M c Bartlett, Scott P a,b Katowitz, James A a,b Zackai, Elaine H a,b

a CHILDREN S HOSPITAL OF PHILADELPHIA (United States)

b UNIVERSITY OF PENNSYLVANIA (United States)

c UNIVERSITY MEDICAL CENTER UTRECHT (Netherlands)

Author keywords

Ablepharon Macrostomia syndrome; Autosomal dominant inheritance

Indexed keywords

ABLEPHARON MACROSTOMIA SYNDROME; ARTICLE; CASE REPORT; CLINICAL FEATURE; CRANIOFACIAL MORPHOLOGY; DISEASE ASSOCIATION; FEMALE; HEAD CIRCUMFERENCE; HUMAN; INFANT; MALFORMATION SYNDROME; MEDICAL HISTORY; NIPPLE MALFORMATION; PHENOTYPE; PRIORITY JOURNAL; SKIN DISEASE; SYNDACTYLY;

ABNORMALITIES, MULTIPLE; EYE ABNORMALITIES; FACIES; FEMALE; HUMANS; INFANT, NEWBORN; MACROSTOMIA; PHENOTYPE;

EID: 81955161924 PISSN: 15524825 EISSN: 15524833 Source Type: Journal
DOI: 10.1002/ajmg.a.34287 Document Type: Article

Times cited : (17)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.