Overlap between VACTERL and hemifacial microsomia illustrating a spectrum of malformations seen in axial mesodermal dysplasia complex (AMDC)

American Journal of Medical Genetics

Volumn 121 A, Issue 2, 2003, Pages 151-155

  Bergmann, Carsten ^a   Zerres, Klaus ^a   Peschgens, Thomas ^a   Senderek, Jan ^a   Hörnchen, Helmut ^a   Rudnik Schöneborn, Sabine ^a  

^a RWTH AACHEN UNIVERSITY   (Germany)

Author keywords

Axial mesodermal dysplasia complex; Hemifacial microsomia; Oculo auriculovertebral spectrum (OAV); Primary developmental field defect; VACTERL

Indexed keywords

ARTICLE; AXIAL MESODERMAL DYSPLASIA COMPLEX; CASE REPORT; CELL MIGRATION; CLINICAL FEATURE; CONGENITAL HEART DISEASE; CONSANGUINEOUS MARRIAGE; ESOPHAGUS ATRESIA; FACE MALFORMATION; HEMIFACIAL MICROSOMIA; HUMAN; KIDNEY MALFORMATION; LIMB DEFECT; LYMPHOCYTE TRANSFORMATION; MALE; MULTIPLE MALFORMATION SYNDROME; NEWBORN; PHENOTYPE; PRIORITY JOURNAL; RIB MALFORMATION; SKELETON MALFORMATION; SYNDROME DELINEATION; SYNDROME VACTERL; SYNDROME VATER; UROGENITAL TRACT MALFORMATION; VERTEBRA MALFORMATION; VISUAL FIELD DEFECT;

EID: 0042193658     PISSN: 15524825     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.a.20167     Document Type: Article

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