MODED: Microcephaly-oculo-digito-esophageal-duodenal syndrome

American Journal of Medical Genetics

Volumn 71, Issue 3, 1997, Pages 251-257

  Frydman, M ^a   Katz, M ^a   Cabot, S G ^a   Soen, G ^a   Kauschansky, A ^a   Sirota, L ^a  

^a GERTNER INSTITUTE FOR EPIDEMIOLOGY AND HEALTH POLICY RESEARCH   (Israel)

Author keywords

Autosomal dominant inheritance; Brachydactyly; Brachymesophalangy; Congenital heart disease; Deafness; Duodenal atresia; Learning disabilities; Mental retardation; Microcephaly; Short stature; Short toes

Indexed keywords

ARTICLE; BRACHYDACTYLY; CLINICAL FEATURE; CONGENITAL MALFORMATION; DIAGNOSTIC APPROACH ROUTE; FAMILIAL DISEASE; FEMALE; HALLUX VALGUS; HUMAN; HUMAN CELL; HUMAN TISSUE; LEARNING DISORDER; MALE; MICROCEPHALY; MODED SYNDROME; PATENT DUCTUS ARTERIOSUS; PHENOTYPE; PRIORITY JOURNAL; SHORT STATURE; SYNDROME DELINEATION;

ABNORMALITIES, MULTIPLE; ADULT; CHILD; CHILD, PRESCHOOL; DUODENUM; ESOPHAGEAL ATRESIA; FEMALE; FINGERS; HUMANS; HYPERTELORISM; INFANT; INFANT, NEWBORN; LEARNING DISORDERS; MALE; MICROCEPHALY; PEDIGREE; PHENOTYPE; SYNDROME; TOES;

VALGUS;

EID: 0030843742     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19970822)71:3<251::AID-AJMG1>3.0.CO;2-X     Document Type: Article

References (14)