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Results:
1-16
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Results: 16
Authors:
Hicsonmez, G
Cetin, M
Yenicesu, I
Olcay, L
Koc, A
Aktas, D
Tuncbilek, E
Tuncer, KM
Citation: G. Hicsonmez et al., Evaluation of children with myelodysplastic syndrome: Importance of extramedullary disease as a presenting symptom, LEUK LYMPH, 42(4), 2001, pp. 665-674
Authors:
Aktas, D
Tuncbilek, E
Onderoglu, L
Citation: D. Aktas et al., Chromosomal mosaicism in a pregnant woman treated with acyclovir for herpes simplex encephalitis, AM J PERIN, 18(4), 2001, pp. 179-183
Authors:
Aktas, D
Tuncbilek, E
Cetin, M
Hicsonmez, G
Citation: D. Aktas et al., Tetrasomy 8 as a primary chromosomal abnormality in a child with acute megakaryoblastic leukemia: a case report and review of the literature, CANC GENET, 126(2), 2001, pp. 166-168
Authors:
Aktas, D
Ozen, H
Atsu, N
Tekin, A
Sozen, S
Tuncbilek, E
Citation: D. Aktas et al., Glutathione S-transferase M1 gene polymorphism in bladder cancer patients:a marker for invasive bladder cancer?, CANC GENET, 125(1), 2001, pp. 1-4
Authors:
Gungor, N
Boke, B
Belgin, E
Tuncbilek, E
Citation: N. Gungor et al., High frequency hearing loss in Ullrich-Turner syndrome, EUR J PED, 159(10), 2000, pp. 740-744
Authors:
Aktas, D
Koc, A
Boduroglu, K
Hicsonmez, G
Tuncbilek, E
Citation: D. Aktas et al., Myelodysplastic syndrome associated with monosomy 7 in a child with Bloom syndrome, CANC GENET, 116(1), 2000, pp. 44-46
Authors:
Tuncbilek, E
Alikasifoglu, M
Aktas, D
Duman, F
Yanik, H
Anar, B
Oostra, B
Willemsen, R
Citation: E. Tuncbilek et al., Screening for the fragile X syndrome among mentally retarded males by hairroot analysis, AM J MED G, 95(2), 2000, pp. 105-107
Authors:
Tokgozoglu, S
Alikasifoglu, M
Unsal, I
Atalar, E
Aytemir, K
Ozer, N
Ovunc, K
Usal, O
Kes, S
Tuncbilek, E
Citation: S. Tokgozoglu et al., Methylene tetrahydrofolate reductase genotype and the risk and extent of coronary artery disease in a population with low plasma folate, HEART, 81(5), 1999, pp. 518-522
Authors:
Boduroglu, K
Tuncbilek, E
Citation: K. Boduroglu et E. Tuncbilek, Frontometaphyseal dysplasia: A case with Arnold-Chiari malformation and bracket epiphysis of the first metacarpal bone, PEDIATR INT, 41(2), 1999, pp. 181-183
Authors:
Koc, A
Oner, R
Oner, C
Aktas, D
Sozen, M
Tuncbilek, E
Altay, C
Citation: A. Koc et al., Myelodysplastic syndrome (MDS) associated with increased hemoglobin F and trisomy 8: presentation of a patient, HEM CELL TH, 41(4), 1999, pp. 187-189
Authors:
Boduroglu, K
Alikasifoglu, M
Anar, B
Tuncbilek, E
Citation: K. Boduroglu et al., Association of the 677C -> T mutation on the methylenetetrahydrofolate reductase gene in turkish patients with neural tube defects, J CHILD NEU, 14(3), 1999, pp. 159-161
Authors:
Aktas, D
Yenicesu, I
Hicsonmez, G
Tuncbilek, E
Citation: D. Aktas et al., Loss of maternal allele in a child with myelodysplastic syndrome and monosomy 7, AM J HEMAT, 62(1), 1999, pp. 49-51
Authors:
Ozen, S
Alikasifoglu, M
Saatci, U
Bakkaloglu, A
Besbas, N
Kara, N
Kocak, H
Erbas, B
Unsal, I
Tuncbilek, E
Citation: S. Ozen et al., Implications of certain genetic polymorphisms in scarring in vesicoureteric reflux: Importance of ACE polymorphism, AM J KIDNEY, 34(1), 1999, pp. 140-145
Authors:
Alikasifoglu, M
Topaloglu, H
Tuncbilek, E
Ceviz, M
Anar, B
Demir, E
Ozme, S
Citation: M. Alikasifoglu et al., Clinical and genetic correlate in childhood onset Friedreich ataxia, NEUROPEDIAT, 30(2), 1999, pp. 72-76
Authors:
Tuncbilek, E
Alikasifoglu, M
Boduroglu, K
Aktas, D
Anar, B
Citation: E. Tuncbilek et al., Frequency of fragile X syndrome among Turkish patients with mental retardation of unknown etiology, AM J MED G, 84(3), 1999, pp. 202-203
Authors:
Erbas, T
Alikasifoglu, M
Aksoyek, S
Unsal, I
Gedik, O
Tuncbilek, E
Citation: T. Erbas et al., Effects of angiotensin-converting enzyme gene polymorphism on the left-ventricular function and mass in patients with acromegaly, CARDIOLOGY, 92(4), 1999, pp. 226-231
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