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Results: 1-12 |
Results: 12
Patterns of inter- and intra-group genetic diversity in the Vlax Roma as revealed by Y chromosome and mitochondrial DNA lineages
Authors: Kalaydjieva, L Calafell, F Jobling, MA Angelicheva, D de Knijff, P Rosser, ZH Hurles, ME Underhill, P Tournev, I Marushiakova, E Popov, V
Citation: L. Kalaydjieva et al., Patterns of inter- and intra-group genetic diversity in the Vlax Roma as revealed by Y chromosome and mitochondrial DNA lineages, EUR J HUM G, 9(2), 2001, pp. 97-104
Hereditary motor and sensory neuropathy-Russe: New autosomal recessive neuropathy in Balkan gypsies
Authors: Thomas, PK Kalaydjieva, L Youl, B Rogers, T Angelicheva, D King, RHM Guergueltcheva, V Colomer, J Lupu, C Corches, A Popa, G Merlini, L Shmarov, A Muddle, JR Nourallah, M Tournev, I
Citation: Pk. Thomas et al., Hereditary motor and sensory neuropathy-Russe: New autosomal recessive neuropathy in Balkan gypsies, ANN NEUROL, 50(4), 2001, pp. 452-457
Origins and divergence of the Roma (Gypsies)
Authors: Gresham, D Morar, B Underhill, PA Passarino, G Lin, AA Wise, C Angelicheva, D Calafell, F Oefner, PJ Shen, PD Tournev, I de Pablo, R Kucinskas, V Perez-Lezaun, A Marushiakova, E Popov, V Kalaydjieva, L
Citation: D. Gresham et al., Origins and divergence of the Roma (Gypsies), AM J HU GEN, 69(6), 2001, pp. 1314-1331
C283Y mutation and other C-terminal nucleotide changes in the gamma-sarcoglycan gene in the Bulgarian gypsy population (vol 14, pg 40, 1999)
Authors: Todorova, A Ashikov, A Beltcheva, O Tournev, I Kremensky, I
Citation: A. Todorova et al., C283Y mutation and other C-terminal nucleotide changes in the gamma-sarcoglycan gene in the Bulgarian gypsy population (vol 14, pg 40, 1999), HUM MUTAT, 15(5), 2000, pp. 479-479
Hereditary motor and sensory neuropathy Lom (HMSNL): refined genetic mapping in Romani (Gypsy) families from several European countries
Authors: Chandler, D Angelicheva, D Heather, L Gooding, R Gresham, D Yanakiev, P de Jonge, R Baas, F Dye, D Karagyozov, L Savov, A Blechschmidt, K Keats, B Thomas, PK King, RHM Starr, A Nikolova, A Colomer, J Ishpekova, B Tournev, I Urtizberea, JA Merlini, L Butinar, D Chabrol, B Voit, T Baethmann, M Nedkova, V Corches, A Kalaydjieva, L
Citation: D. Chandler et al., Hereditary motor and sensory neuropathy Lom (HMSNL): refined genetic mapping in Romani (Gypsy) families from several European countries, NEUROMUSC D, 10(8), 2000, pp. 584-591
Homogeneous phenotype of the gypsy limb-girdle MD with the gamma-sarcoglycan C283Y mutation
Authors: Merlini, L Kaplan, JC Navarro, C Barois, A Bonneau, D Brasa, J Echenne, B Gallano, P Jarre, L Jeanpierre, M Kalaydjieva, L Leturcq, F Levi-Gomes, A Toutain, A Tournev, I Urtizberea, A Vallat, JM Voit, T Warter, JM
Citation: L. Merlini et al., Homogeneous phenotype of the gypsy limb-girdle MD with the gamma-sarcoglycan C283Y mutation, NEUROLOGY, 54(5), 2000, pp. 1075-1079
A novel locus for autosomal recessive peripheral neuropathy in the EGR2 region on 10q23
Authors: Rogers, T Chandler, D Angelicheva, D Thomas, PK Youl, B Tournev, I Gergelcheva, V Kalaydjieva, L
Citation: T. Rogers et al., A novel locus for autosomal recessive peripheral neuropathy in the EGR2 region on 10q23, AM J HU GEN, 67(3), 2000, pp. 664-671
C283Y mutation and other C-terminal nucleotide changes in the gamma-sarcoglycan gene in the Bulgarian Gypsy population
Authors: Todorova, A Ashikov, A Beltcheva, O Tournev, I Kremensky, I
Citation: A. Todorova et al., C283Y mutation and other C-terminal nucleotide changes in the gamma-sarcoglycan gene in the Bulgarian Gypsy population, HUM MUTAT, 14(1), 1999, pp. 40-44
Congenital cataracts facial dysmorphism neuropathy syndrome, a novel complex genetic disease in Balkan gypsies: Clinical and electrophysiological observations
Authors: Tournev, I Kalaydjieva, L Youl, B Ishpekova, B Guergueltcheva, V Kamenov, O Katzarova, M Kamenov, Z Raicheva-Terzieva, M King, RHM Romanski, K Petkov, R Schmarov, A Dimitrova, G Popova, N Uzunova, M Milanov, S Petrova, J Petkov, Y Kolarov, G Aneva, L Radeva, O Thomas, PK
Citation: I. Tournev et al., Congenital cataracts facial dysmorphism neuropathy syndrome, a novel complex genetic disease in Balkan gypsies: Clinical and electrophysiological observations, ANN NEUROL, 45(6), 1999, pp. 742-750
Ultrastructural changes in peripheral nerve in hereditary motor and sensory neuropathy-Lom
Authors: King, RHM Tournev, I Colomer, J Merlini, L Kalaydjieva, L Thomas, PK
Citation: Rhm. King et al., Ultrastructural changes in peripheral nerve in hereditary motor and sensory neuropathy-Lom, NEUROP AP N, 25(4), 1999, pp. 306-312
A founder mutation in the GK1 gene is responsible for galactokinase deficiency in Roma (Gypsies)
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
Peripheral nerve abnormalities in the congenital cataracts facial dysmorphism neuropathy (CCFDN) syndrome
Authors: Tournev, I King, RHM Workman, J Nourallah, M Muddle, JR Kalaydjieva, L Romanski, K Thomas, PK
Citation: I. Tournev et al., Peripheral nerve abnormalities in the congenital cataracts facial dysmorphism neuropathy (CCFDN) syndrome, ACT NEUROP, 98(2), 1999, pp. 165-170
Risultati: 1-12 |