Feingold syndrome: Clinical review and genetic mapping

American Journal of Medical Genetics

Volumn 122 A, Issue 4, 2003, Pages 294-300

  Celli, Jacopo ^a   Van Bokhoven, Hans ^a   Brunner, Han G ^a  

^a RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

Author keywords

Duodenal atresia; Esophageal atresia; Hydronephrosis; Sonic hedgehog; VATER VAC TERL association

Indexed keywords

SONIC HEDGEHOG PROTEIN;

ANUS ATRESIA; AUTOSOMAL DOMINANT INHERITANCE; CHROMOSOME 2P; CHROMOSOME MAP; CLINICAL FEATURE; CLINODACTYLY; CONFERENCE PAPER; CONGENITAL HEART MALFORMATION; DUODENUM ATRESIA; ESOPHAGUS ATRESIA; FEINGOLD SYNDROME; HUMAN; HYDRONEPHROSIS; LIMB MALFORMATION; MAJOR CLINICAL STUDY; MICROCEPHALY; MULTIPLE MALFORMATION SYNDROME; PRIORITY JOURNAL; SIGNAL TRANSDUCTION; SYNDACTYLY; VERTEBRA MALFORMATION;

ERINACEIDAE;

EID: 0141993865     PISSN: 15524825     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.a.20471     Document Type: Conference Paper

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