Gene localisation to 12q2 in the atrio-digital Holt-Oram syndrome;LOCALISATION D'UN GENE DU SYNDROME ATRIO-DIGITAL DE HOLT-ORAM EN 12Q2

Archives des Maladies du Coeur et des Vaisseaux

Volumn 88, Issue 5, 1995, Pages 661-666

  Bonnet, D ^a   Terrett, J ^a   Pequignot Viegas, E ^a   Weissenbach, J ^a   Munnich, A ^a   Lyonnet, S ^a   Kachaner, J ^a  

^a HÔPITAL NECKER ENFANTS MALADES   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CHROMOSOME 12Q; CLINICAL ARTICLE; CONGENITAL HEART DISEASE; GENE LOCATION; HEART ATRIUM SEPTUM DEFECT; HOLT ORAM SYNDROME; HUMAN; MORPHOGENESIS; PHENOTYPE; RADIOGRAPHY; CHROMOSOME 12; CHROMOSOME MAP; CONGENITAL HEART MALFORMATION; CONGENITAL MALFORMATION; FEMALE; FINGER; GENETICS; HEART SEPTUM DEFECT; MALE; PEDIGREE; REVIEW; SYNDROME;

CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 12; ENGLISH ABSTRACT; FEMALE; FINGERS; HEART DEFECTS, CONGENITAL; HEART SEPTAL DEFECTS, ATRIAL; HUMAN; MALE; PEDIGREE; SYNDROME;

EID: 0029009494     PISSN: 00039683     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (0)