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Citation: I. Eisenberg et al., The UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene ismutated in recessive hereditary inclusion body myopathy, NAT GENET, 29(1), 2001, pp. 83-87

Authors: Eisenberg, I Hochner, H Shemesh, M Levi, T Potikha, T Sadeh, M Argov, Z Jackson, CL Mitrani-Rosenbaum, S

Citation: I. Eisenberg et al., Physical and transcriptional map of the hereditary inclusion body myopathylocus on chromosome 9p12-p13, EUR J HUM G, 9(7), 2001, pp. 501-509

Authors: Amsalem, H Tsvieli, R Zentner, BS Yagel, S Mitrani-Rosenbaum, S Hurwitz, A

Citation: H. Amsalem et al., Monopaternal superfecundation of quintuplets after transfer of two embryosin an in vitro fertilization cycle, FERT STERIL, 76(3), 2001, pp. 621-623

Authors: Avner, R Wahrman, J Richler, C Ayoub, N Friedmann, A Laufer, N Mitrani-Rosenbaum, S

Citation: R. Avner et al., X inactivation-specific transcript expression in mouse oocytes and zygotes, MOL HUM REP, 6(7), 2000, pp. 591-594

Authors: Argov, Z Sadeh, M Mazor, K Soffer, D Kahana, E Eisenberg, I Mitrani-Rosenbaum, S Richard, I Beckmann, J Keers, S Bashir, R Bushby, K Rosenmann, H

Citation: Z. Argov et al., Muscular dystrophy due to dysferlin deficiency in Libyan Jews - Clinical and genetic features, BRAIN, 123, 2000, pp. 1229-1237

Authors: Eisenberg, I Thiel, C Levi, T Tiram, E Argov, Z Sadeh, M Jackson, CL Thierfelder, L Mitrani-Rosenbaum, S

Citation: I. Eisenberg et al., Fine-structure mapping of the hereditary inclusion body myopathy locus, GENOMICS, 55(1), 1999, pp. 43-48