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Whole exome sequencing and array-based molecular karyotyping as aids to prenatal diagnosis in fetuses with suspected Simpson-Golabi-Behmel syndrome.
Kehrer, Christina; Hoischen, Alexander; Menkhaus, Ralf; Schwab, Eva; Müller, Andreas; Kim, Sarah; Kreiß, Martina; Weitensteiner, Valerie; Hilger, Alina; Berg, Christoph; Geipel, Anne; Reutter, Heiko; Gembruch, Ulrich.
Affiliation
  • Kehrer C; Department of Obstetrics and Prenatal Medicine, University of Bonn, Bonn, Germany.
  • Hoischen A; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.
  • Menkhaus R; Center for Assisted Reproduction and Prenatal Diagnosis, Minden, Germany.
  • Schwab E; Medical Office for Human Genetics, Wiesbaden, Germany.
  • Müller A; Department of Neonatology and Pediatric Intensive Care, University of Bonn, Bonn, Germany.
  • Kim S; Institute of Human Genetics, University of Bonn, Bonn, Germany.
  • Kreiß M; Institute of Human Genetics, University of Bonn, Bonn, Germany.
  • Weitensteiner V; Institute of Human Genetics, University of Bonn, Bonn, Germany.
  • Hilger A; Institute of Human Genetics, University of Bonn, Bonn, Germany.
  • Berg C; Department of Obstetrics and Prenatal Medicine, University of Bonn, Bonn, Germany.
  • Geipel A; Department of Obstetrics and Prenatal Medicine, University of Bonn, Bonn, Germany.
  • Reutter H; Department of Neonatology and Pediatric Intensive Care, University of Bonn, Bonn, Germany.
  • Gembruch U; Institute of Human Genetics, University of Bonn, Bonn, Germany.
Prenat Diagn ; 36(10): 961-965, 2016 Oct.
Article in En | MEDLINE | ID: mdl-27589329
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Arrhythmias, Cardiac / Abnormalities, Multiple / Genetic Diseases, X-Linked / Gigantism / Heart Defects, Congenital / Intellectual Disability Type of study: Diagnostic_studies / Etiology_studies Limits: Adult / Female / Humans / Male / Newborn / Pregnancy Language: En Journal: Prenat Diagn Year: 2016 Document type: Article Affiliation country: Germany Country of publication: United kingdom
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Arrhythmias, Cardiac / Abnormalities, Multiple / Genetic Diseases, X-Linked / Gigantism / Heart Defects, Congenital / Intellectual Disability Type of study: Diagnostic_studies / Etiology_studies Limits: Adult / Female / Humans / Male / Newborn / Pregnancy Language: En Journal: Prenat Diagn Year: 2016 Document type: Article Affiliation country: Germany Country of publication: United kingdom