Review of genetic factors in intestinal malrotation

Pediatric Surgery International

Volumn 26, Issue 8, 2010, Pages 769-781

  Martin, Vicki ^a,b   Shaw Smith, Charles ^a,b  

^a WELLCOME TRUST SANGER INSTITUTE   (United Kingdom)

^b UNIVERSITY COLLEGE LONDON   (United Kingdom)

Author keywords

Embryology; FOXF1; Genetics; Intestinal malrotation

Indexed keywords

FORKHEAD TRANSCRIPTION FACTOR;

ANUS ATRESIA; AUTOSOMAL DOMINANT INHERITANCE; AUTOSOMAL RECESSIVE DISORDER; CASE REPORT; CHROMOSOME; ESOPHAGUS ATRESIA; GALLBLADDER AGENESIS; GENE LOCUS; GENE MUTATION; HEREDITY; HIRSCHSPRUNG DISEASE; HUMAN; INTESTINE MALROTATION; MESENTERIC ARTERY; MORPHOLOGY; PANCREAS MALFORMATION; PRIORITY JOURNAL; REVIEW; TRACHEOESOPHAGEAL FISTULA; UMBILICAL CORD; X CHROMOSOME LINKED DISORDER;

ACTIVIN RECEPTORS, TYPE II; CONTRACTILE PROTEINS; DIGESTIVE SYSTEM ABNORMALITIES; FORKHEAD TRANSCRIPTION FACTORS; HOMEODOMAIN PROTEINS; HUMANS; INFANT, NEWBORN; INTERCELLULAR SIGNALING PEPTIDES AND PROTEINS; INTESTINES; LEFT-RIGHT DETERMINATION FACTORS; MICROFILAMENT PROTEINS; MUTATION; RISK FACTORS; SYNDROME; TRANSCRIPTION FACTORS;

EID: 77955557170     PISSN: 01790358     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00383-010-2622-5     Document Type: Review

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