Deletion 22q11 in patients with interrupted aortic arch

American Journal of Cardiology

Volumn 84, Issue 3, 1999, Pages 360-361

  Marino, Bruno ^a   Digilio, Maria Cristina ^a   Persiani, Monica ^a   Di Donato, Roberto ^a   Toscano, Alessandra ^a   Giannotti, Aldo ^a   Dallapiccola, Bruno ^b  

^a Cardiac Surg Med Genet B   (Italy)

^b UNIVERSITY OF ROME TOR VERGATA   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

AORTA ARCH INTERRUPTION; ARTICLE; CHROMOSOME 22Q; CHROMOSOME ANALYSIS; CHROMOSOME DELETION; CLINICAL ARTICLE; DIGEORGE SYNDROME; DISEASE ASSOCIATION; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE LOCUS; HUMAN; INFANT; MALE; MORPHOGENESIS; PHENOTYPE; PRESCHOOL CHILD; PRIORITY JOURNAL;

ABNORMALITIES, MULTIPLE; AORTA, THORACIC; AORTIC DISEASES; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 22; FEMALE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT; INFANT, NEWBORN; MALE;

EID: 0033180446     PISSN: 00029149     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0002-9149(99)00297-0     Document Type: Article

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