Prenatal diagnosis of conotroncal cardiac disease: Results in 337 cases;Diagnostic prenatal des cardiopathies conotroncales. A propos de 337 cas

Archives des Maladies du Coeur et des Vaisseaux

Volumn 93, Issue 5, 2000, Pages 583-586

  Boudjemline, Y ^a   Fermont, L ^a   Le Bidois, J ^a   Fraisse, A ^a   Kachaner, J ^a   Villain, E ^a   Sidi, D ^a   Bonnet, D ^a  

^a NONE

Author keywords

[No Author keywords available]

Indexed keywords

AORTA COARCTATION; AORTOPULMONARY SEPTAL DEFECT; ARTICLE; ATRESIA; CHROMOSOME 22Q; CHROMOSOME DELETION; CONGENITAL HEART MALFORMATION; ECHOGRAPHY; FALLOT TETRALOGY; FETUS; GREAT BLOOD VESSEL; GREAT VESSELS TRANSPOSITION; HEART VENTRICLE SEPTUM DEFECT; HUMAN; INCIDENCE; KARYOTYPE; LUNG ATRESIA; MAJOR CLINICAL STUDY; PRENATAL DIAGNOSIS; PULMONARY VALVE DISEASE; SECOND TRIMESTER PREGNANCY; CARDIOVASCULAR MALFORMATION; CHROMOSOME 22; CHROMOSOME ABERRATION; FEMALE; GENETICS; HEART SEPTUM DEFECT; KARYOTYPING; PREGNANCY; PRENATAL DEVELOPMENT;

CARDIOVASCULAR ABNORMALITIES; CHROMOSOME ABERRATIONS; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 22; FEMALE; HEART DEFECTS, CONGENITAL; HEART SEPTAL DEFECTS, VENTRICULAR; HUMANS; KARYOTYPING; PREGNANCY; PREGNANCY TRIMESTER, SECOND; PULMONARY ATRESIA; TETRALOGY OF FALLOT; ULTRASONOGRAPHY, PRENATAL;

EID: 0034063360     PISSN: 00039683     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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