Genetic factors in isolated and syndromic esophageal atresia

Journal of Pediatric Gastroenterology and Nutrition

Volumn 52, Issue SUPPL. 1, 2011, Pages

  Geneviève, David ^a   De Pontual, Loïc ^b   Amiel, Jeanne ^b   Lyonnet, Stanislas ^b  

^a HÔPITAL ARNAUD DE VILLENEUVE   (France)

^b HÔPITAL NECKER ENFANTS MALADES   (France)

Author keywords

[No Author keywords available]

Indexed keywords

CARBIMAZOLE; DOXORUBICIN; MITOCHONDRIAL DNA; SONIC HEDGEHOG PROTEIN; TRANSCRIPTION FACTOR SOX2;

ARTICLE; BARTSOCAS PAPAS SYNDROME; CLINICAL FEATURE; CONGENITAL MALFORMATION; DNA DAMAGE; DNA REPAIR; ESOPHAGUS ATRESIA; FANCONI ANEMIA; FEINGOLD SYNDROME; FETAL ALCOHOL SYNDROME; FOX1 GENE; FOXF1 GENE; FRYNS SYNDROME; GENE; GENE CLUSTER; GENE MUTATION; GENETIC DISORDER; GLI2 GENE; GLI3 GENE; HEREDITY; HOXC4 GENE; HUMAN; ISOLATED ESOPHAGEAL ATRESIA; MATERNAL DIABETES MELLITUS; MENTAL DEFICIENCY; MOUSE; MULTIPLE CONGENITAL ANOMALY; NOGGIN GENE; NONHUMAN; OPITZ SYNDROME; PCSK5 GENE; PHENYLKETONURIA; PRIORITY JOURNAL; ROGERS SYNDROME; SYNDROME CHARGE; SYNDROME VACTERL; SYNDROMIC ESOPHAGEAL ATRESIA; TRISOMY 13; TRISOMY 18; TRISOMY 21; TTF1 GENE;

ANAL CANAL; ANEMIA, MEGALOBLASTIC; CHARGE SYNDROME; CHROMOSOME ABERRATIONS; DIABETES MELLITUS; DUODENAL OBSTRUCTION; ENVIRONMENTAL EXPOSURE; ESOPHAGEAL ATRESIA; ESOPHAGUS; EYELIDS; FANCONI ANEMIA; FEMALE; HEARING LOSS, SENSORINEURAL; HEART DEFECTS, CONGENITAL; HUMANS; KETOGLUTARATE DEHYDROGENASE COMPLEX; KIDNEY; LIMB DEFORMITIES, CONGENITAL; MATERNAL EXPOSURE; MICROCEPHALY; MUTATION; PREGNANCY; SPINE; TRACHEA; TRACHEOESOPHAGEAL FISTULA;

EID: 79955567635     PISSN: 02772116     EISSN: None     Source Type: Journal    
DOI: 10.1097/MPG.0b013e318213316a     Document Type: Article

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