Blastogenesis dominant 1: A sequence with midline anomalies and heterotaxy

American Journal of Medical Genetics

Volumn 68, Issue 4, 1997, Pages 405-408

  De Meeus, Anne ^a   Sarda, Pierre ^c   Tenconi, Romano ^b   Ferrière, Marc ^c   Bouvagnet, Patrice ^a,c  

^a Centre National de la Recherche Scientifique   (France)

^b Servizio di Genetica Medica   (Italy)

^c HÔPITAL ARNAUD DE VILLENEUVE   (France)

Author keywords

autosomal dominant; blastogenesis; cardiac malformation; lateralization defect; midline

Indexed keywords

ADULT; ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; BLASTOGENESIS DOMINANT 1 DISORDER; CHILD; CLINICAL ARTICLE; CONGENITAL HEART MALFORMATION; CONGENITAL MALFORMATION; DIAPHRAGM HERNIA; FEMALE; HUMAN; LATERALIZATION DEFECT; MALE; NEWBORN; PRIORITY JOURNAL; THORAX MALFORMATION; URINARY TRACT MALFORMATION;

ABNORMALITIES, MULTIPLE; ADULT; BLASTOCYST; CHILD, PRESCHOOL; CORPUS CALLOSUM; EMBRYONIC AND FETAL DEVELOPMENT; EYE; FEMALE; GENES, DOMINANT; HEART DEFECTS, CONGENITAL; HUMANS; INFANT, NEWBORN; INTESTINES; KIDNEY; MALE; PEDIGREE; PRENATAL DIAGNOSIS; UROGENITAL ABNORMALITIES; UROGENITAL SYSTEM;

EID: 0031019373     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19970211)68:4<405::AID-AJMG6>3.0.CO;2-K     Document Type: Article

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