Clinical

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Comprehensive genetic analysis to identify causative mutations of diseases in the field of pediatric surgery


ABSTRACT: Primary outcome(s): Identification of causative mutations suggesting possible involvement in the development of each pediatric surgical disease

DISEASE(S): Congenital Digestive Tract Atresia, Gastrointestinal Motility Disorder, Intestinal Malrotation, Congenital Gastrointestinal Malformation, Hirschsprung Disease, Anorectal Malformation, Neonatal Gastrointestinal Perforation, Pancreaticobiliary Maljunction, Biliary Atresia, Portal Hypertension, Liver Fibrosis, Congenital Airway Disease, Pulmonary Cystic Disease, Diaphragmatic Hernia, Vascular Or Lymphatic Malformation, Tumor Disease, Abdominal Wall Dysplasia, Renal Urological Malformation, Malformation Syndrome, Etc

PROVIDER: 2653767 | ecrin-mdr-crc |

REPOSITORIES: ECRIN MDR

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