机译:先天性簇生肠病的遗传表征:EPCAM相关表型和纺锤氮中的参与综合征
Department of Pediatric Gastroenterology Hepatology and Nutrition Necker-Enfants Malades Hospital;
Department of Pediatric Gastroenterology Hepatology and Nutrition Necker-Enfants Malades Hospital;
Department of Pathology Necker-Enfants Malades Hospital Université Paris Descartes 75015 Paris;
Department of Pathology Necker-Enfants Malades Hospital Université Paris Descartes 75015 Paris;
Department of Pediatric Nutrition and Gastroenterology Armand-Trousseau Hospital Pierre et Marie;
Department of Pediatric Nutrition and Gastroenterology Armand-Trousseau Hospital Pierre et Marie;
Department of Pathology Armand-Trousseau Hospital Pierre et Marie Curie University 75012 Paris;
Department of Pediatric Gastroenterology Robert Debré Hospital Université Paris Diderot 75019;
Department of Pediatric Gastroenterology Robert Debré Hospital Université Paris Diderot 75019;
Department of Pediatric Gastroenterology Hepatology and Nutrition Necker-Enfants Malades Hospital;
Department of Opthalmology Necker-Enfants Malades Hospital Université Paris Descartes 75015;
Department of Opthalmology Necker-Enfants Malades Hospital Université Paris Descartes 75015;
Department of Dermatology Necker-Enfants Malades Hospital Université Paris Descartes 75015 Paris;
Department of Pediatric Gastroenterology Hepatology and Nutrition Necker-Enfants Malades Hospital;
Department of Pediatric Gastroenterology Hepatology and Nutrition Necker-Enfants Malades Hospital;
Department of Pediatric Gastroenterology Hepatology and Nutrition Necker-Enfants Malades Hospital;
Department of Pediatric Gastroenterology Hepatology and Nutrition Necker-Enfants Malades Hospital;
Institut Imagine INSERM U989 Université Paris Descartes 75015 Paris France;
Department of Pediatrics i Innsbruck Medical University Innsbruck Austria;
Department of Pediatrics i Innsbruck Medical University Innsbruck Austria;
Clinical Medical Center Dr. von Haunersches Kinderspital Ludwig Maximilians University Munich;
Institut Imagine INSERM U781 Université Paris Descartes 75015 Paris France;
Institut Imagine INSERM U781 Université Paris Descartes 75015 Paris France;
Institut Imagine INSERM U781 Université Paris Descartes 75015 Paris France;
Institut Jacques Monod CNRS University Paris Diderot 75205 Paris France;
Institut Imagine INSERM U781 Université Paris Descartes 75015 Paris France;
机译:先天簇状肠病的遗传特征:Epcam相关表型和SPINT2以综合征形式出现
机译:在先天性钠腹泻中见到簇状肠病的病例带有SPINT2突变。
机译:EPCAM突变更新:与先天性簇生肠病和林奇综合征相关的变体
机译:先天性变形和稀有遗传综合征的耳蜗植入:Goldenhar和Branchio-Oculo-Facial
机译:对Peters Plus综合征和先天性障碍的分子机制调查重叠表型
机译:病征簇绒肠病港口spINT2突变的情况下先天性腹泻看到钠
机译:先天性腹泻/簇生肠道中鉴定的纺丝体(HAI-2)麦克信变异影响Hai-2抑制前列腺素但不是矩阵酶的能力