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Silverstein, S
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Falik-Zaccai, TC
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Lerer, I
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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
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Kaduri, L
Gibs, M
Hubert, A
Sagi, M
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Weinberg, N
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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
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Buiting, K
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Dworniczak, B
Lerer, I
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Temple, IK
Harvey, JF
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Gross, S
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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
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