Absent pulmonary valve with intact ventricular septum and patent ductus arteriosus: A specific cardiac phenotype associated with deletion 18q syndrome [2]

American Journal of Medical Genetics

Volumn 138 A, Issue 2, 2005, Pages 185-186

  Versacci, Paolo ^a   Digilio, M Cristina ^b   Sauer, Ursula ^c   Dallapiccola, Bruno ^a   Marino, Bruno ^a  

^a SAPIENZA UNIVERSITY OF ROME   (Italy)

^b BAMBINO GESÙ CHILDREN S HOSPITAL   (Italy)

^c TECHNICAL UNIVERSITY OF MUNICH   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

CASE REPORT; CHROMOSOME 18Q; DISEASE ASSOCIATION; GENE DELETION; GENE LOCATION; HEART VENTRICLE SEPTUM; HUMAN; INFANT; LETTER; MALE; PATENT DUCTUS ARTERIOSUS; PHENOTYPE; PRIORITY JOURNAL; PULMONARY VALVE DISEASE; RARE DISEASE;

ABNORMALITIES, MULTIPLE; ADOLESCENT; CHILD; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 18; DUCTUS ARTERIOSUS, PATENT; ECHOCARDIOGRAPHY; FEMALE; HEART SEPTAL DEFECTS; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT; KARYOTYPING; MALE; PULMONARY VALVE; SYNDROME;

EID: 25644446922     PISSN: 15524825     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.a.30916     Document Type: Letter

References (12)

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