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Results: 1-4 |
Results: 4

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: 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: Kalaydjieva, L Perez-Lezaun, A Angelicheva, D Onengut, S Dye, D Bosshard, NU Jordanova, A Savov, A Yanakiev, P Kremensky, I Radeva, B Hallmayer, J Markov, A Nedkova, V Tournev, I Aneva, L Gitzelmann, R
Citation: L. Kalaydjieva et al., A founder mutation in the GK1 gene is responsible for galactokinase deficiency in Roma (Gypsies), AM J HU GEN, 65(5), 1999, pp. 1299-1307

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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