Patent ductus arteriosus and microdeletion 22q11 in a patient with Klinefelter syndrome

Annales de Genetique

Volumn 43, Issue 2, 2000, Pages 105-107

  Velagaleti, Gopalrao V N ^a   Kumar, Anil ^a   Lockhart, Lillian H ^a   Matalon, Reuben ^a  

^a University of Texas Medical Branch School of Medicine   (United States)

Author keywords

Deletion 22q11; Klinefelter syndrome; Patent ductus arteriosus

Indexed keywords

ADULT; ARTICLE; CASE REPORT; CHROMOSOME 22Q; CHROMOSOME DELETION; CONGENITAL HEART DISEASE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; HUMAN CELL; KARYOTYPE; KLINEFELTER SYNDROME; LYMPHOCYTE; MALE; PATENT DUCTUS ARTERIOSUS;

EID: 0033798430     PISSN: 00033995     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0003-3995(00)01013-3     Document Type: Article

References (7)

1. Chromosome 22q11 deletion syndrome: An update and review for the primary physician
2. Congenital heart disease in 49,XXXXY syndrome
3. Atypical electrocardiogram and echocardiogram in a patient with Bland-White-Garland syndrome m association with atrial septal defect
4. Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: A European collaborative study
5. Genetic disorders associated with overgrowth
6. An elderly man with Klinefelter syndrome associated with hypertrophic cardiomyopathy, sick sinus syndrome, and coronary arteriovenous fistula