HLA-DPB1, -DRB1, and -DQB1 polymorphism defined in Ewenki ethnic minority of China Inner Mongolia Autonomous Region von Su, X., Bi, L., Hai, R., Qimuge, S., Ying, M., Bahring, S., Gong, M.

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A new mutation in the elastin gene causing supravalvular aortic stenosis von Boeckel, Thomas, Dierks, Astrid, Vergopoulos, Athanasios, Bähring, Sylvia, Knoblauch, Hans, Müller-Myhsok, Bertram, Baron, Heike, Aydin, Atakan, Bein, Georg, Luft, Friedrich C, Schuster, Herbert

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A cis-regulatory site downregulates PTHLH in translocation t(8;12)(q13;p11.2) and leads to Brachydactyly Type E von Maass, Philipp G., Wirth, Jutta, Aydin, Atakan, Rump, Andreas, Stricker, Sigmar, Tinschert, Sigrid, Otero, Miguel, Tsuchimochi, Kaneyuki, Goldring, Mary B., Luft, Friedrich C., Bähring, Sylvia

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Deletion at 12p in a Japanese child with brachydactyly overlaps the assigned locus of brachydactyly with hypertension in a Turkish family von Bähring, S, Nagai, T, Toka, H R, Nitz, I, Toka, O, Aydin, A, Mühl, A, Wienker, T F, Schuster, H, Luft, F C

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Serum- and Glucocorticoid-Regulated Kinase (SGK1) Gene and Blood Pressure von Busjahn, Andreas, Aydin, Atakan, Uhlmann, Regina, Krasko, Christine, Bähring, Sylvia, Szelestei, Tamas, Feng, Yuxi, Dahm, Stephan, Sharma, Arya M, Luft, Friedrich C, Lang, Florian

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A Cholesterol-Lowering Gene Maps to Chromosome 13q von Knoblauch, Hans, Müller-Myhsok, Bertram, Busjahn, Andreas, Avi, Liat Ben, Bähring, Sylvia, Baron, Heike, Heath, Simon C., Uhlmann, Regina, Faulhaber, Hans-Dieter, Shpitzen, Shoshi, Aydin, Atakan, Reshef, Ayeleth, Rosenthal, Magda, Eliav, Osnat, Mühl, Astrid, Lowe, Adam, Schurr, Danny, Harats, Dror, Jeschke, Evi, Friedlander, Yechiel, Schuster, Herbert, Luft, Friedrich C., Leitersdorf, Eran

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A phage T7 class-III promoter functions as a polymerase II promoter in mammalian cells von Sandig, Volker, Lieber, Andre, Bähring, Sylvia, Strauss, Michael

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Severe autosomal dominant hypertension and brachydactyly in a unique Turkish kindred maps to human chromosome 12 von Schuster, Herbert, Wienker, Thomas F, Bähring, Sylvia, Bilginturan, Nihat, Toka, Hakan R, Neitzel, Heidemarie, Jeschke, Eva, Toka, Okan, Gilbert, Dennis, Lowe, Adam, Ott, Jürg, Haller, Hermann, Luft, Friedrich C

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Single nucleotide polymorphism map of five long-QT genes von Aydin, Atakan, Bähring, Sylvia, Dahm, Stefan, Guenther, Ulf P, Uhlmann, Regina, Busjahn, Andreas, Luft, Friedrich C

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Serum levels of l-arginine analogues and glutathione peroxidase and catalase gene variants in Type 2 diabetes mellitus patients von Szelestei, T., Bähring, S., Wagner, Z., Aydin, A., Molnár, G. A., Kocsis, B., Nagy, J., Wittmann, I.

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Neurovascular compression at the ventrolateral medulla in autosomal dominant hypertension and brachydactyly von NARAGHI, R, SCHUSTER, H, HALLER, H, FAHLBUSCH, R, LUFT, F. C, TOKA, H. R, BÄHRING, S, TOKA, O, ÖZTEKIN, Ö, BILGINTURAN, N, KNOBLAUCH, H, WIENKER, T. F, BUSJAHN, A

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Oligonucleotide ligation assay (OLA) for the diagnosis of familial hypercholesterolemia von Baron, Heike, Fung, Steven, Aydin, Atakan, Bähring, Sylvia, Luft, Friedrich C, Schuster, Herbert

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Association of a uteroglobin polymorphism with rate of progression in patients with IgA nephropathy von Szelestei, Tamás, Bähring, Sylvia, Kovács, Tibor, Vas, Tibor, Salamon, Csaba, Busjahn, Andreas, Luft, Friedrich C., Nagy, Judit

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New universal primers facilitate Pyrosequencing von Aydin, Atakan, Toliat, Mohammad R., Bähring, Sylvia, Becker, Christian, Nürnberg, Peter

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Mutation in the ARH Gene and a Chromosome 13q Locus Influence Cholesterol Levels in a New Form of Digenic-Recessive Familial Hypercholesterolemia von Al-Kateb, Hussam, Bähring, Sylvia, Hoffmann, Katrin, Strauch, Konstantin, Busjahn, Andreas, Nürnberg, Gudrun, Jouma, Muhidien, Bautz, Eckehard K.F, Dresel, Hans A, Luft, Friedrich C

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Autosomal Dominant Hypertension and Brachydactyly in a Turkish Kindred Resembles Essential Hypertension von Schuster, Herbert, Wienker, Thomas F, Toka, Hakan R, Bahring, Sylvia, Jeschke, Eva, Toka, Okan, Busjahn, Andreas, Hempel, Albrecht, Tahlhammer, Christoph, Oelkers, Wolfgang, Kunze, Jurgen, Bilginturan, Nihat, Haller, Hermann, Luft, Friedrich C

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Autosomal-Dominant Hypertension With Type E Brachydactyly Is Caused by Rearrangement on the Short Arm of Chromosome 12 von Bähring, Sylvia, Rauch, Anita, Toka, Okan, Schroeder, Christoph, Hesse, Christiane, Siedler, Heike, Fesüs, Gabor, Haefeli, Walter E, Busjahn, Andreas, Aydin, Atakan, Neuenfeld, Yvette, Mühl, Astrid, Toka, Hakan R, Gollasch, Maik, Jordan, Jens, Luft, Friedrich C

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Validation of fluorescence-labeled artificial nonhuman sequences for single-strand conformation polymorphism mutation detection in familial hypercholesterolemia von Aydin, Atakan, Luft, Friedrich C., Bähring, Sylvia

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Efficient and Cost-Effective Single Nucleotide Polymorphism Detection with Different Fluorescent Applications von Aydin, A, Baron, H, Bähring, S, Schuster, H, Luft, F.C

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Quantitative trait loci for blood pressure exist near the IGF-1, the Liddle syndrome, the angiotensin II-receptor gene and the renin loci in man von NAGY, Z, BUSJAHN, A, BÄHRING, S, FAULHABER, H.-D, GOHLKE, H.-R, KNOBLAUCH, H, ROSENTHAL, M, MÜLLER-MYHSOK, B, SCHUSTER, H, LUFT, F. C

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