Associated malformations in patients with esophageal atresia

European Journal of Medical Genetics

Volumn 52, Issue 5, 2009, Pages 287-290

  Stoll, Claude ^a   Alembik, Yves ^a   Dott, Beatrice ^a   Roth, Marie Paule ^a  

^a UNIVERSITÉ DE STRASBOURG   (France)

Author keywords

Congenital malformations; Esophageal atresia; Tracheooesophageal fistula

Indexed keywords

ARTICLE; CARDIOVASCULAR MALFORMATION; CENTRAL NERVOUS SYSTEM MALFORMATION; CHROMOSOME ABERRATION; CONGENITAL MALFORMATION; DIGESTIVE SYSTEM MALFORMATION; DISEASE ASSOCIATION; ESOPHAGUS ATRESIA; FANCONI ANEMIA; FETUS; FRYNS SYNDROME; GENETIC ASSOCIATION; GOLDENHAR SYNDROME; HUMAN; MAJOR CLINICAL STUDY; MUSCULOSKELETAL SYSTEM MALFORMATION; NEWBORN; OPITZ SYNDROME; PREVALENCE; SIRENOMELIA; SYNDROME CHARGE; UROGENITAL TRACT MALFORMATION;

ABNORMALITIES, MULTIPLE; ABORTION, INDUCED; CHROMOSOME ABERRATIONS; CITIES; COHORT STUDIES; CONGENITAL ABNORMALITIES; ESOPHAGEAL ATRESIA; FEMALE; FRANCE; HUMANS; INFANT, NEWBORN; LIVE BIRTH; PREGNANCY; PREVALENCE; REGISTRIES; RETROSPECTIVE STUDIES; RURAL POPULATION; STILLBIRTH; URBAN POPULATION;

FISTULA;

EID: 68949115965     PISSN: 17697212     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ejmg.2009.04.004     Document Type: Article

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