Alagille syndrome in a family with duplication 20p11

Clinical Dysmorphology

Volumn 5, Issue 4, 1996, Pages 279-288

  Moog, U ^a   Engelen, J ^a   Albrechts, J ^a   Hoorntje, T ^a   Hendrikse, F ^a   Schrander Stumpel, C ^a  

^a MAASTRICHT UNIVERSITY   (Netherlands)

Author keywords

Alagille syndrome; arteriohepatic dysplasia; duplication 20p11; pulmonary valve atresia

Indexed keywords

ADULT; ALAGILLE SYNDROME; ARTICLE; CASE REPORT; CHROMOSOME 20P; CHROMOSOME DUPLICATION; HUMAN; HUMAN CELL; IN SITU HYBRIDIZATION; INFANT; MALE; PRIORITY JOURNAL;

EID: 0029780416     PISSN: 09628827     EISSN: None     Source Type: Journal    
DOI: 10.1097/00019605-199610000-00001     Document Type: Article

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