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Results: 1-10 |
Results: 10
A deletion/insertion mutation in the BRCA2 gene in a breast cancer family:A possible role of the Alu-polyA tail in the evolution of the deletion
Authors: Wang, T Lerer, I Gueta, Z Sagi, M Kadouri, L Peretz, T Abeliovich, D
Citation: T. Wang et al., A deletion/insertion mutation in the BRCA2 gene in a breast cancer family:A possible role of the Alu-polyA tail in the evolution of the deletion, GENE CHROM, 31(1), 2001, pp. 91-95
CAG and GGC repeat polymorphisms in the androgen receptor gene and breast cancer susceptibility in BRCA1/2 carriers and non-carriers
Authors: Kadouri, L Easton, DF Edwards, S Hubert, A Kote-Jarai, Z Glaser, B Durocher, F Abeliovich, D Peretz, T Eeles, RA
Citation: L. Kadouri et al., CAG and GGC repeat polymorphisms in the androgen receptor gene and breast cancer susceptibility in BRCA1/2 carriers and non-carriers, BR J CANC, 85(1), 2001, pp. 36-40
The 28-kb deletion spanning D15S63 is a polymorphic variant in the Ashkenazi Jewish population
Authors: Silverstein, S Lerer, I Buiting, K Abeliovich, D
Citation: S. Silverstein et al., The 28-kb deletion spanning D15S63 is a polymorphic variant in the Ashkenazi Jewish population, AM J HU GEN, 68(1), 2001, pp. 261-263
X inactivation phenotype in carriers of Pelizaeus-Merzbacher disease: skewed in carriers of a duplication and random in carriers of point mutations
Authors: Woodward, K Kirtland, K Dlouhy, S Raskind, W Bird, T Malcolm, S Abeliovich, D
Citation: K. Woodward et al., X inactivation phenotype in carriers of Pelizaeus-Merzbacher disease: skewed in carriers of a duplication and random in carriers of point mutations, EUR J HUM G, 8(6), 2000, pp. 449-454
Contribution of connexin 26 mutations to nonsyndromic deafness in Ashkenazi patients and the variable phenotypic effect of the mutation 167delT
Authors: Lerer, I Sagi, M Malamud, E Levi, H Raas-Rothschild, A Abeliovich, D
Citation: I. Lerer et al., Contribution of connexin 26 mutations to nonsyndromic deafness in Ashkenazi patients and the variable phenotypic effect of the mutation 167delT, AM J MED G, 95(1), 2000, pp. 53-56
Genetic testing of breast and ovarian cancer patients: clinical characteristics and hormonal risk modifiers
Authors: Kaduri, L Gibs, M Hubert, A Sagi, M Heching, N Lerer, I Uziely, B Weinberg, N Abeliovich, D Peretz, T
Citation: L. Kaduri et al., Genetic testing of breast and ovarian cancer patients: clinical characteristics and hormonal risk modifiers, EUR J OB GY, 85(1), 1999, pp. 75-80
Clinical implications of fluorescence in situ hybridization analysis in 13chronic myeloid leukemia cases: Ph-negative and variant Ph-positive
Authors: Yehuda, O Abeliovich, D Ben-Neriah, S Sverdlin, I Cohen, R Varadi, G Orr, R Ashkenazi, YJ Heyd, J Lugassy, G Ben Yehuda, D
Citation: O. Yehuda et al., Clinical implications of fluorescence in situ hybridization analysis in 13chronic myeloid leukemia cases: Ph-negative and variant Ph-positive, CANC GENET, 114(2), 1999, pp. 100-107
Multiple chromosomal abnormalities in fulminant anaplastic myeloma
Authors: Maslovsky, I Lugassy, G Blumental, R Ducach, A Yehuda, O Abeliovich, D
Citation: I. Maslovsky et al., Multiple chromosomal abnormalities in fulminant anaplastic myeloma, CLIN LAB H, 21(3), 1999, pp. 207-210
A 28-kb deletion spanning D15S63 (PW71) in five families: A rare neutral variant?
Authors: Buiting, K Dittrich, B Dworniczak, B Lerer, I Abeliovich, D Cottrell, S Temple, IK Harvey, JF Lich, C Gross, S Horsthemke, B
Citation: K. Buiting et al., A 28-kb deletion spanning D15S63 (PW71) in five families: A rare neutral variant?, AM J HU GEN, 65(6), 1999, pp. 1588-1594
The Jewish Ashkenazi founder mutations in the BRCA1/BRCA2 genes are not found at an increased frequency in Ashkenazi patients with prostate cancer
Authors: Hubert, A Peretz, T Manor, O Kaduri, L Wienberg, N Lerer, I Sagi, M Abeliovich, D
Citation: A. Hubert et al., The Jewish Ashkenazi founder mutations in the BRCA1/BRCA2 genes are not found at an increased frequency in Ashkenazi patients with prostate cancer, AM J HU GEN, 65(3), 1999, pp. 921-924
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