Expansion of the genotypic and phenotypic spectrum in patients with KRAS germline mutations

Journal of Medical Genetics - Tập 44 Số 2 - Trang 131-135
Martin Zenker1, Katarina Lehmann2, AL Schulz3, Heidi Barth4, D. Hansmann5, Rainer Koenig6, Rudolf Korinthenberg7, Martina Kreiß‐Nachtsheim8, Peter Meinecke9, Susanne Morlot10, Stefan Mundlos2, Anne S. Quante11, Salmo Raskin12, Dirk Schnabel13, Lore Wehner14, Christian P. Kratz7, Denise Horn2, Kerstin Kutsche15
1Institute of Human Genetics, University of Erlangen-Nuremberg, Germany
2Institute of Medical Genetics, Charité, University Medicine of Berlin, Germany
3Institut für Humangenetik, Universitätsklinikum Hamburg-Eppendorf, Hamburg, Germany;
4Zentrum für Kinder-und Jugendmedizin, Klinik für Neonatologie und Neuropädiatrie, Marburg, Germany
5Pränatalmedizin und Medizinische Genetik, Meckenheim, Germany
6Institute of Human Genetics, University of Frankfurt, Germany
7Department of Paediatrics and Adolescent Medicine, University of Freiburg, Germany
8Institute of Human Genetics, Friedrich-Wilhelms-University of Bonn, Germany
9Medizinische Genetik, Altonaer Kinderkrankenhaus, Hamburg, Germany
10Praxis für Humangenetik, Ärztliche Partnerschaft Wagner-Stibbe Hannover, Germany
11Institute of Human Genetics, Heinrich-Heine-University of Düsseldorf, Germany
12Laboratorio Genetika, Alameda Augusto Stellfeld, Curitiba Parana, Brazil
13Institute of Paediatric Endocrinology, University Children's Hospital, University Medicine of Berlin, Germany
14Institute of Human Genetics, University of Göttingen, Germany
15Universitätsklinikum Hamburg-Eppendorf, Butenfeld 42, 22529 Hamburg, Germany

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Journal of Medical Genetics

Tập 44 Số 2

131-135

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