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Hempelmann S. Kumar S. Muralitharan T. Sander July 01, 2006 / Hum Genet Medullary cystic kidney disease type 1: mutational analysis in 37 genes based on haplotype sharing M.T. Wolf B.E. Mucha H.C. Hennies M. Attanasio F. Panther I. Zalewski S.M. Karle E.A. Otto C.C. Deltas A. Fuchshuber F. Hildebrandt June 01, 2006 / Audiol Neuro-Otol Neurotological and neuroanatomical changes in the connexin-26-related HID/KID syndrome I. Todt H.C. Hennies W. Kuester J. Smolle G. Rademacher S. Mutze D. Basta A. Eisenschenk A. Ernst May 01, 2006 / Epilepsy Res Evaluation of CACNA1H in European patients with childhood absence epilepsy B. Chioza K. Everett H. Aschauer O. Brouwer P. Callenbach A. Covanis O. Dulac M. Durner O. Eeg-Olofsson M. Feucht M. Friis A. Heils M. Kjeldsen K. Larsson A.E. Lehesjoki R. Nabbout I. Olsson T. Sander A. Siren R. Robinson M. Rees R.M. Gardiner June 01, 2006 / Mamm Genome Integrated gene expression profiling and linkage analysis in the rat E. Petretto J. Mangion M. Pravanec N. Hubner T.J. Aitman January 01, 2006 Gene chip technology and its application to molecular medicine H. Zimdahl N. Hübner May 22, 2006 / Mol Vis A novel fan-shaped cataract-microcornea syndrome caused by a mutation of CRYAA in an Indian family V. Vanita J.R. Singh J.F. Hejtmancik P. Nuernberg H.C. Hennies D. Singh K. Sperling October 11, 2006 / Physiol Genomics Reciprocal congenic lines for a major stroke-QTL on rat chromosome 1 S. Rubattu N. Hubner U. Ganten A. Evangelista R. Stanzione E.D. Angelantonio R. Plehm R. Langanki E. Gianazza L. Sironi G. D'Amati M. Volpe October 01, 2006 / Am J Med Genet A Diagnostic yield of various genetic approaches in patients with unexplained developmental delay or mental retardation A. Rauch J. Hoyer S. Guth C. Zweier C. Kraus C. Becker M. Zenker U. Hueffmeier C. Thiel F. Rueschendorf P. Nuernberg A. Reis U. Trautmann September 15, 2006 / Hum Mol Genet Evidence for involvement of the vitamin D receptor gene in idiopathic short stature via a genome-wide linkage study and subsequent association studies A. Dempfle S.A. Wudy K. Saar S. Hagemann S. Friedel A. Scherag L.D. Berthold G. Alzen L. Gortner W.F. Blum A. Hinney P. Nuernberg H. Schaefer J. Hebebrand Pagination Current page 1 Page 2 Page 3 Page 4 … Next page Next › Last page Last »
July 10, 2006 / Neurosci Lett Myofibrillogenesis regulator 1 gene (MR-1) mutation in an Omani family with paroxysmal nonkinesigenic dyskinesia A. Hempelmann S. Kumar S. Muralitharan T. Sander
July 01, 2006 / Hum Genet Medullary cystic kidney disease type 1: mutational analysis in 37 genes based on haplotype sharing M.T. Wolf B.E. Mucha H.C. Hennies M. Attanasio F. Panther I. Zalewski S.M. Karle E.A. Otto C.C. Deltas A. Fuchshuber F. Hildebrandt
June 01, 2006 / Audiol Neuro-Otol Neurotological and neuroanatomical changes in the connexin-26-related HID/KID syndrome I. Todt H.C. Hennies W. Kuester J. Smolle G. Rademacher S. Mutze D. Basta A. Eisenschenk A. Ernst
May 01, 2006 / Epilepsy Res Evaluation of CACNA1H in European patients with childhood absence epilepsy B. Chioza K. Everett H. Aschauer O. Brouwer P. Callenbach A. Covanis O. Dulac M. Durner O. Eeg-Olofsson M. Feucht M. Friis A. Heils M. Kjeldsen K. Larsson A.E. Lehesjoki R. Nabbout I. Olsson T. Sander A. Siren R. Robinson M. Rees R.M. Gardiner
June 01, 2006 / Mamm Genome Integrated gene expression profiling and linkage analysis in the rat E. Petretto J. Mangion M. Pravanec N. Hubner T.J. Aitman
May 22, 2006 / Mol Vis A novel fan-shaped cataract-microcornea syndrome caused by a mutation of CRYAA in an Indian family V. Vanita J.R. Singh J.F. Hejtmancik P. Nuernberg H.C. Hennies D. Singh K. Sperling
October 11, 2006 / Physiol Genomics Reciprocal congenic lines for a major stroke-QTL on rat chromosome 1 S. Rubattu N. Hubner U. Ganten A. Evangelista R. Stanzione E.D. Angelantonio R. Plehm R. Langanki E. Gianazza L. Sironi G. D'Amati M. Volpe
October 01, 2006 / Am J Med Genet A Diagnostic yield of various genetic approaches in patients with unexplained developmental delay or mental retardation A. Rauch J. Hoyer S. Guth C. Zweier C. Kraus C. Becker M. Zenker U. Hueffmeier C. Thiel F. Rueschendorf P. Nuernberg A. Reis U. Trautmann
September 15, 2006 / Hum Mol Genet Evidence for involvement of the vitamin D receptor gene in idiopathic short stature via a genome-wide linkage study and subsequent association studies A. Dempfle S.A. Wudy K. Saar S. Hagemann S. Friedel A. Scherag L.D. Berthold G. Alzen L. Gortner W.F. Blum A. Hinney P. Nuernberg H. Schaefer J. Hebebrand