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American Journal of Medical Genetics. Part A|April 6, 2011
A deleterious mutation in the LOXHD1 gene causes autosomal recessive hearing loss in Ashkenazi JewsS Edvardson, C Jalas, A Shaag, et al.Genes, Chromosomes & Cancer|April 3, 2001
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 deletionT Wang, I Lerer, Z Gueta, et al.European Journal of Human Genetics : EJHG|January 1, 1996
Cystic fibrosis heterozygote screening in the Orthodox Community of Ashkenazi Jews: the Dor Yesharim approach and heterozygote frequencyD Abeliovich, A Quint, N Weinberg, et al.American Journal of Human Genetics|June 1, 1993
Negative expansion of the myotonic dystrophy unstable sequenceD Abeliovich, I Lerer, I Pashut-Lavon, et al.Biulleten' Eksperimental'Noi Biologii I Meditsiny|May 1, 1992
[Effects of human defensin HNP-1 on the production of tumor necrosis factor-alpha by human blood monocytes in vitro]N I Misuno, T S Kolesnikova, R I Lerer, et al.Human Molecular Genetics|June 1, 1994
Detection of aberrant DNA methylation in unique Prader-Willi syndrome patients and its diagnostic implicationsK Buiting, B Dittrich, W P Robinson, et al.Clinical Endocrinology|March 14, 1998
Sporadic phaeochromocytomas are rarely associated with germline mutations in the von Hippel-Lindau and RET genesM Bar, E Friedman, O Jakobovitz, et al.Cancer Genetics and Cytogenetics|January 1, 1996
Predominant 45,X,--Y karyotype in donor cells after allogeneic BMT: cytogenetic and molecular analysisD Abeliovich, O Yehuda, A Nagler, et al.American Journal of Medical Genetics|December 1, 1994
Neurofibromatosis type I (NFI) in Israeli families: linkage analysis as a diagnostic toolS Elyakim, I Lerer, J Zlotogora, et al.Cancer Genetics and Cytogenetics|October 15, 1991
"Jumping translocation" in a 17-month-old child with mixed-lineage leukemiaS Ben-Neriah, A Abramov, I Lerer, et al.Pageof 5