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Results: 1-20 |
Results: 20

Authors: Hertz, JM Juncker, I Persson, U Matthijs, G Schmidtke, J Petersen, MB Kjeldsen, M Gregersen, N
Citation: Jm. Hertz et al., Detection of mutations in the COL4A5 gene by SSCP in X-linked Alport syndrome, HUM MUTAT, 18(2), 2001, pp. 141-148

Authors: Sauermann, U Nurnberg, P Bercovitch, FB Berard, JD Trefilov, A Widdig, A Kessler, M Schmidtke, J Krawczak, M
Citation: U. Sauermann et al., Increased reproductive success of MHC class II heterozygous males among free-ranging rhesus macaques, HUM GENET, 108(3), 2001, pp. 249-254

Authors: Stuhrmann, M Bashawri, L Ahmed, MA Al-Awamy, BH Kuhnau, W Schmidtke, J El-Harith, EA
Citation: M. Stuhrmann et al., Familial thrombocytosis as a recessive, possibly X-linked trait in an Arabfamily, BR J HAEM, 112(3), 2001, pp. 616-620

Authors: Krawczak, M Cooper, DN Schmidtke, J
Citation: M. Krawczak et al., Estimating the efficacy and efficiency of cascade genetic screening, AM J HU GEN, 69(2), 2001, pp. 361-370

Authors: Ludecke, HJ Schaper, J Meinecke, P Momeni, P Gross, S von Holtum, D Hirche, H Abramowicz, MJ Albrecht, B Apacik, C Christen, HJ Claussen, U Devriendt, K Fastnacht, E Forderer, A Friedrich, U Goodship, THJ Greiwe, M Hamm, H Hennekam, RCM Hinkel, GK Hoeltzenbein, M Kayserili, H Majewski, F Mathieu, M McLeod, R Midro, AT Moog, U Nagai, T Niikawa, N Orstavik, KH Plochl, E Seitz, C Schmidtke, J Tranebjaerg, L Tsukahara, M Wittwer, B Zabel, B Gillessen-Kaesbach, G Horsthemke, B
Citation: Hj. Ludecke et al., Genotypic and phenotypic spectrum in tricho-rhino-phalangeal syndrome types I and III, AM J HU GEN, 68(1), 2001, pp. 81-91

Authors: Aymc, S Bobrow, M Coviello, D Evers-Kiebooms, G Farndon, P Kaariainen, H Kristoffersson, U Pembrey, M Raeburn, S Cassiman, JJ Schmidtke, J ten Kate, L Tranebjaerg, L
Citation: S. Aymc et al., Population genetic screening programmes: Proposed recommendations of the European Society of Human Genetics (vol 8, pg 998, 2000), EUR J HUM G, 8(12), 2000, pp. 998-1000

Authors: Schubert, S Dechend, F Skawran, B Kunze, B Winking, H Weile, C Romer, I Hemberger, M Fundele, R Sharma, T Schmidtke, J
Citation: S. Schubert et al., Silencing of the Y-chromosomal gene tspy during murine evolution, MAMM GENOME, 11(4), 2000, pp. 288-291

Authors: Langen, H von Kietzell, D Byrd, D Arslan-Kirchner, M Vester, U Stuhrmann, M Dork, T Saar, K Reis, A Schmidtke, J Brodehl, J
Citation: H. Langen et al., Renal polyamine excretion, tubular amino acid reabsorption and molecular genetics in cystinuria, PED NEPHROL, 14(5), 2000, pp. 376-384

Authors: Stuhrmann, M Graf, N Dork, T Schmidtke, J
Citation: M. Stuhrmann et al., Mutation screening for prenatal and presymptomatic diagnosis: cystic fibrosis and haemochromatosis, EUR J PED, 159, 2000, pp. S186-S191

Authors: Dechend, F Williams, G Skawran, B Schubert, S Krawczak, M Tyler-Smith, C Schmidtke, J
Citation: F. Dechend et al., TSPY variants in six loci on the human Y chromosome, CYTOG C GEN, 91(1-4), 2000, pp. 67-71

Authors: Schubert, S Dechend, F Skawran, B Krawczak, M Schmidtke, J
Citation: S. Schubert et al., Molecular evolution of the murine tspy genes, CYTOG C GEN, 91(1-4), 2000, pp. 239-242

Authors: Schmidtke, J Stille, W Strobl, G
Citation: J. Schmidtke et al., Static and dynamic light scattering of a nematic side-group polysiloxane, MACROMOLEC, 33(8), 2000, pp. 2922-2928

Authors: Tascou, S Nayernia, K Samani, A Schmidtke, J Vogel, T Engel, W Burfeind, P
Citation: S. Tascou et al., Immortalization of murine male germ cells at a discrete stage of differentiation by a novel directed promoter-based selection strategy, BIOL REPROD, 63(5), 2000, pp. 1555-1561

Authors: Trefilov, A Berard, J Krawczak, M Schmidtke, J
Citation: A. Trefilov et al., Natal dispersal in rhesus macaques is related to serotonin transporter gene promoter variation, BEHAV GENET, 30(4), 2000, pp. 295-301

Authors: El-Harith, EA Abdel-Hadi, MS Doerk, T Badr, AN Schmidtke, J
Citation: Ea. El-harith et al., The potential benefits of genetic testing in breast and ovarian cancer, SAUDI MED J, 20(9), 1999, pp. 663-670

Authors: Borgmann, S Luhmer, I Arslan-Kirchner, M Kallfelz, HC Schmidtke, J
Citation: S. Borgmann et al., A search for chromosome 22q11.2 deletions in a series of 176 consecutivelycatheterized patients with congenital heart disease: no evidence for deletions in non-syndromic patients, EUR J PED, 158(12), 1999, pp. 958-963

Authors: Trefilov, A Krawczak, M Berard, J Schmidtke, J
Citation: A. Trefilov et al., DNA sequence polymorphisms in genes involved in the regulation of dopamineand serotonin metabolism in rhesus macaques, ELECTROPHOR, 20(8), 1999, pp. 1771-1777

Authors: El-Harith, EA Kuhnau, W Schmidtke, J Stuhrmann, M Nasserallah, Z Al-Shahri, A
Citation: Ea. El-harith et al., Identification and clinical presentation of beta thalassaemia mutations inthe eastern region of Saudi Arabia, J MED GENET, 36(12), 1999, pp. 935-937

Authors: Schmidtke, J Manns, MP
Citation: J. Schmidtke et Mp. Manns, Genetic diseases in internal medicine, INTERNIST, 40(5), 1999, pp. 467-468

Authors: Dechend, F Schubert, S Nanda, I Vogel, T Schmid, M Schmidtke, J
Citation: F. Dechend et al., Organization and expression of rat Tspy, CYTOG C GEN, 83(3-4), 1998, pp. 270-274
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