Research output per year
Research output per year
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Dive into the research topics where Boleslaw Goldman is active. These topic labels come from the works of this person. Together they form a unique fingerprint.
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Preimplantation genetic haplotyping a new application for diagnosis of translocation carrier's embryos- preliminary observations of two robertsonian translocation carrier families
Shamash, J., Rienstein, S., Wolf-Reznik, H., Pras, E., Dekel, M., Litmanovitch, T., Brengauz, M., Goldman, B., Yonath, H., Dor, J., Levron, J. & Aviram-Goldring, A., Jan 2011, In: Journal of Assisted Reproduction and Genetics. 28, 1, p. 77-83 7 p.Research output: Contribution to journal › Article › peer-review
Open Access14 Scopus citations -
Comprehensive diagnosis of Rett's syndrome relying on genetic, epigenetic and expression evidence of deficiency of the methyl-CpG-binding protein 2 gene: study of a cohort of Israeli patients.
Petel-Galil, Y., Ben-Zeev, B., Greenbaum, I., Vecsler, M., Goldman, B., Lohi, H., Minassian, B. A. & Gak, E., Feb 2007, In: Journal of Medical Genetics. 44, 2, p. e56Research output: Contribution to journal › Article › peer-review
4 Scopus citations -
Erratum: Comprehensive diagnosis of Rett's syndrome relying on genetic, epigenetic and expression evidence of deficiency of the methyl-CpG-binding protein 2 gene: Study of a cohort of Israeli patients (Journal of Medical Genetics (2006) 43, (e56))
Petel-Galil, Y., Ben-Zeev, B., Greenbaum, I., Vecsler, M., Goldman, B., Lohi, H., Minassian, B. A. & Gak, E., Feb 2007, In: Journal of Medical Genetics. 44, 2, p. 147 1 p.Research output: Contribution to journal › Comment/debate
Open Access -
Combined genetic profiles of components and regulators of the vitamin K-dependent γ-carboxylation system affect individual sensitivity to warfarin
Vecsler, M., Loebstein, R., Almog, S., Kurnik, D., Goldman, B., Halkin, H. & Gak, E., Feb 2006, In: Thrombosis and Haemostasis. 95, 2, p. 205-211 7 p.Research output: Contribution to journal › Article › peer-review
149 Scopus citations -
Comprehensive diagnosis of Rett's syndrome relying on genetic, epigenetic and expression evidence of deficiency of the methyl-CpG-binding protein 2 gene: study of a cohort of Israeli patients.
Petel-Galil, Y., Benteer, B., Galil, Y. P., Zeev, B. B., Greenbaum, I., Vecsler, M., Goldman, B., Lohi, H., Minassian, B. A. & Gak, E., Dec 2006, In: Journal of Medical Genetics. 43, 12, p. e56Research output: Contribution to journal › Letter › peer-review
Open Access9 Scopus citations