Feingold syndrome: Report of a new family and review

American Journal of Medical Genetics

Volumn 73, Issue 1, 1997, Pages 55-60

  Courtens, W ^a   Levi, S ^a   Verbelen, F ^b   Verloes, A ^c   Vamos, E ^a  

^a BRUGMANN UNIVERSITY HOSPITAL   (Belgium)

^b First Line Medical Care ^*  (Belgium)

^c UNIVERSITY OF LIÈGE   (Belgium)

Author keywords

Brachymesophalangy of fifth fingers; Duodenal atresia; Feingold syndrome; Learning disabilities; Microcephaly; Oesophageal atresia; Syndactyly of toes 4 5 2 3

Indexed keywords

ARTICLE; CASE REPORT; DUODENUM ATRESIA; ESOPHAGUS ATRESIA; FACE MALFORMATION; FAMILIAL DISEASE; FEINGOLD SYNDROME; HUMAN; INFANT; MALE; MICROCEPHALY; PRIORITY JOURNAL; SYNDACTYLY; TRACHEOESOPHAGEAL FISTULA;

ABNORMALITIES, MULTIPLE; ADULT; DUODENAL DISEASES; ESOPHAGEAL ATRESIA; FACE; FEMALE; FOOT DEFORMITIES, CONGENITAL; HAND DEFORMITIES, CONGENITAL; HUMANS; INFANT, NEWBORN; MALE; PEDIGREE; SYNDROME;

FISTULA; RAPHIA FRATER;

EID: 0030725244     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19971128)73:1<55::AID-AJMG11>3.0.CO;2-Q     Document Type: Article

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