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Analytics & Computing Resequencing

Resequencing homepage Projects Information Request form Contact: info@resequencing.mpg.de

Current and Past NGFN and DHGP II Projects DNAH5: chromosome 5p - primary ciliary dyskinesia and randomization of left-right asymmetry with H. Omran Department of Pediatrics and Adolescent Medicine, Albert Ludwigs University, Freiburg, Germany NPHP3: chromosome 3q - human adolescent nephronophthisis with H. Omran Department of Pediatrics and Adolescent Medicine, Albert Ludwigs University, Freiburg, Germany NPHP4: chromosome 1p - nephronophthisis and retinitis pigmentosa with F. Hildebrandt Department of Pediatrics, University of Michigan, Ann Arbor, MI, USA BSND: chromosome 1p - Bartter syndrome with sensorineural deafness and kidney failure with F. Hildebrandt University Children's Hospital, Freiburg University,Freiburg, Germany DFNA18: chromosome 3q - non-syndromic autosomal-dominant hearing loss with T. Deufel Institut für Klinische Chemie und Laboratoriumsdiagnostik, Klinikum der Friedrich-Schiller Universität Jena, Germany ATP2C1: chromosome 3q - Hailey-Hailey disease with A. Monaco The Wellcome Trust Center For Human Genetics, University of Oxford, UK HTRE1, GABRR1, GABRR2: analysis of positional and functional candidate genes for epilepsy, cooperation with T. Sander, K. Lenzen, Mikrosatelliten-Zentrum, MDC; Berlin, Germany DTNBP1: region is in linkage disequilibrium with schizophrenia ; with D. Wildenauer, Bonn, Germany.

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