Persistent truncus arteriosus in monozygotic twins: Case report and literature review

American Journal of Medical Genetics

Volumn 82, Issue 2, 1999, Pages 146-148

  Mas, C ^a   Delatycki, M B ^a   Weintraub, R G ^a  

^a ROYAL CHILDREN'S HOSPITAL   (Australia)

Author keywords

Deletion 22q11; DiGeorge syndrome; Persistent truncus arteriosus; Twins

Indexed keywords

AORTOPULMONARY SEPTAL DEFECT; ARTICLE; CASE REPORT; CHROMOSOME DELETION; DIGEORGE SYNDROME; FAMILY HISTORY; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; MONOZYGOTIC TWINS; NEWBORN; PEDIGREE; PRIORITY JOURNAL;

DISEASES IN TWINS; FEMALE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT, NEWBORN; MALE; PEDIGREE; TRUNCUS ARTERIOSUS, PERSISTENT; TWINS, MONOZYGOTIC;

EID: 0033555474     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19990115)82:2<146::AID-AJMG9>3.0.CO;2-P     Document Type: Article

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