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Citation: E. Geva et al., The risk of Fragile X premutation expansion is lower in carriers detected by general prenatal screening than in carriers from known Fragile X families, GENET TEST, 4(3), 2000, pp. 289-292

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Citation: M. Horowitz et al., Prevalence of glucocerebrosidase mutations in the Israeli Ashkenazi Jewishpopulation (vol 12, pg 240, 1998), HUM MUTAT, 13(3), 1999, pp. 255-255

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Citation: Y. Nevo et al., Fetal muscle biopsy as a diagnostic tool in Duchenne muscular dystrophy, PRENAT DIAG, 19(10), 1999, pp. 921-926

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Citation: P. Rozen et al., Notable intrafamilial phenotypic variability in a kindred with familial adenomatous polyposis and an APC mutation in exon 9, GUT, 45(6), 1999, pp. 829-833

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Citation: P. Rozen et al., Prevalence of the I1307K APC gene variant in Israeli Jews of differing ethnic origin and risk for colorectal cancer, GASTROENTY, 116(1), 1999, pp. 54-57

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