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Targeted array comparative genomic hybridisation (array CGH) identifies genomic imbalances associated with isolated congenital diaphragmatic hernia (CDH)
Authors:Kasemsri Srisupundit  Paul D Brady  Koenraad Devriendt  Jean-Pierre Fryns  Rogelio Cruz-Martinez  Eduard Gratacos  Jan A Deprest  Joris R Vermeesch
Institution:1. Centre for Human Genetics, K.U. Leuven, Leuven, Belgium

Fetal Medicine Unit, Department of Woman and Child, Division of Gynaecology and Obstetrics, U.Z. Leuven, Leuven, Belgium

Maternal Fetal Medicine Unit, Department of Obstetrics and Gynaecology, Faculty of Medicine, Chiang Mai University, Thailand

These two authors contributed equally to this work.;2. Centre for Human Genetics, K.U. Leuven, Leuven, Belgium

These two authors contributed equally to this work.;3. Centre for Human Genetics, K.U. Leuven, Leuven, Belgium;4. Department of Maternal-Fetal Medicine (ICGON) Hospital Clinic-IDIBAPS, University of Barcelona and Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBER-ER), Barcelona, Spain;5. Fetal Medicine Unit, Department of Woman and Child, Division of Gynaecology and Obstetrics, U.Z. Leuven, Leuven, Belgium

Abstract:
Keywords:congenital diaphragmatic hernia  isolated CDH  array CGH  EFNB1  8p deletions  mosaic trisomy 2  prenatal diagnosis
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