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Results: 1-7 |
Results: 7

Authors: Tolun, A
Citation: A. Tolun, Comment on Holger Breithaupt's article 'Losing them is not an option' in EMBO reports, August 2001, EMBO REP, 2(10), 2001, pp. 860-861

Authors: Rosser,"Efgrafov, O Syrrou, M Meitinger, TA Rubinsztein, DC Stefanescu, G Tolun, A
Citation: O. Rosser,"efgrafov et al., Y-chromosomal diversity in Europe is clinal and influenced primarily by geography, rather than by language (vol 67, pg 1526, 2000), AM J HU GEN, 68(4), 2001, pp. 1075-1075

Authors: Kilinc, MO Ninis, VN Tolun, A Estivill, X Casals, T Savov, A Dagli, E Karakoc, F Demirkol, M Huner, G Ozkinay, F Demir, E Seculi, JL Pena, J Bousono, C Ferrer-Calvete, J Calvo, C Glover, G Kremenski, I
Citation: Mo. Kilinc et al., Genotype-phenotype correlation in three homozygotes and nine compound heterozygotes for the cystic fibrosis mutation 2183AA -> G shows a severe phenotype, J MED GENET, 37(4), 2000, pp. 307-309

Authors: Onengut, S Kavaslar, GN Battaloglu, E Serdaroglu, P Deymeer, F Ozdemir, C Calafell, F Tolun, A
Citation: S. Onengut et al., Deletion pattern in the dystrophin gene in Turks and a comparison with Europeans and Indians, ANN HUM GEN, 64, 2000, pp. 33-40

Authors: Rosser, ZH Zerjal, T Hurles, ME Adojaan, M Alavantic, D Amorim, A Amos, W Armenteros, M Arroyo, E Barbujani, G Beckman, G Beckman, L Bertranpetit, J Bosch, E Bradley, DG Brede, G Cooper, G Corte-Real, HBSM de Knijff, P Decorte, R Dubrova, YE Evgrafov, O Gilissen, A Glisic, S Golge, M Hill, EW Jeziorowska, A Kalaydjieva, L Kayser, M Kivisild, T Kravchenko, SA Krumina, A Kucinskas, V Lavinha, J Livshits, LA Malaspina, P Maria, S McElreavey, K Meitinger, TA Mikelsaar, AV Mitchell, RJ Nafa, K Nicholson, J Norby, S Pandya, A Parik, J Patsalis, PC Pereira, L Peterlin, B Pielberg, G Prata, ML Previdere, C Roewer, L Rootsi, S Rubinsztein, DC Saillard, J Santos, FR Stefanescu, G Sykes, BC Tolun, A Villems, R Tyler-Smith, C Jobling, MA
Citation: Zh. Rosser et al., Y-chromosomal diversity in Europe is clinal and influenced primarily by geography, rather than by language, AM J HU GEN, 67(6), 2000, pp. 1526-1543

Authors: Kavaslar, GN Onengut, S Derman, O Kaya, A Tolun, A
Citation: Gn. Kavaslar et al., The novel genetic disorder microhydranencephaly maps to chromosome 16p13.3-12.1, AM J HU GEN, 66(5), 2000, pp. 1705-1709

Authors: Teraoka, SN Telatar, M Becker-Catania, S Liang, T Onengut, S Tolun, A Chessa, L Sanal, O Bernatowska, E Gatti, RA Concannon, P
Citation: Sn. Teraoka et al., Splicing defects in the ataxia-telangiectasia gene, ATM: Underlying mutations and consequences, AM J HU GEN, 64(6), 1999, pp. 1617-1631
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