Feingold syndrome (MODED syndrome: Microcephaly-oculo-digito-esophageal- duodenal syndrome);Syndrome de Feingold

Archives de Pediatrie

Volumn 7, Issue 6, 2000, Pages 637-640

  Alessandri, J L ^a   Graber, D ^b   Tiran Rajaofera, I ^a   Montbrun, A ^a   Pilorget, H ^a   Samperiz, S ^a   Attali, T ^a   De Napoli Cocci, S ^c  

^a Serv Reanimation Neonatale Pediat   (France)

^b CENTRE HOSPITALIER   (France)

^c Centre Hospitalier Departemental   (France)

Author keywords

Abnormalities; Duodenal diseases, genetics; Esophageal atresia, genetics; Face; Foot deformities, genetics; Hand deformities, genetics; Syndrome, Feingold

Indexed keywords

ADULT; ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CASE REPORT; CLINODACTYLY; DUODENUM ATRESIA; ESOPHAGUS ATRESIA; ESOPHAGUS MALFORMATION; EYE MALFORMATION; FINGER MALFORMATION; GENE MUTATION; GENETIC VARIABILITY; HUMAN; MALE; MALFORMATION SYNDROME; MICROCEPHALY; TOE MALFORMATION;

EID: 0034213642     PISSN: 0929693X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0929-693X(00)80132-3     Document Type: Article

References (12)

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