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Shlomit Rienstein

Showing results (11-20 of 21) with videos related to

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Cancer Genetics and Cytogenetics|April 22, 2009
Genetic alterations detected by comparative genomic hybridization and recurrence rate in epithelial ovarian carcinomaIlan Bruchim, Ofir Israeli, Salaheddin M Mahmud, et al.
Investigative Ophthalmology & Visual Science|November 24, 2006
Mapping of a gene causing brittle cornea syndrome in Tunisian jews to 16q24Almogit Abu, Moshe Frydman, Dina Marek, et al.
Journal of Assisted Reproduction and Genetics|April 19, 2013
Chromosomal integrity of human preimplantation embryos at different days post fertilizationMichal Dekel-Naftali, Ayala Aviram-Goldring, Talia Litmanovitch, et al.
Neurology. Genetics|June 3, 2021
Chromosomal Microarray Analysis in Pregnancies With Corpus Callosum or Posterior Fossa AnomaliesLior Greenbaum, Idit Maya, Lena Sagi-Dain, et al.
Cancer Genetics and Cytogenetics|September 24, 2004
Genomic analyses of primary and metastatic serous epithelial ovarian cancerOfir Israeli, Walter H Gotlieb, Eitan Friedman, et al.
Journal of Neurosurgery|November 8, 2005
Epidermal growth factor receptor gene amplification and expression in disseminated pediatric low-grade gliomasUri Tabori, Shlomit Rienstein, Yaara Dromi, et al.
Journal of Assisted Reproduction and Genetics|September 28, 2010
Preimplantation genetic haplotyping a new application for diagnosis of translocation carrier's embryos- preliminary observations of two robertsonian translocation carrier familiesJana Shamash, Shlomit Rienstein, Haike Wolf-Reznik, et al.
European Journal of Human Genetics : EJHG|June 21, 2012
Screening of human pluripotent stem cells using CGH and FISH reveals low-grade mosaic aneuploidy and a recurrent amplification of chromosome 1qMichal Dekel-Naftali, Ayala Aviram-Goldring, Talia Litmanovitch, et al.
Journal of Perinatal Medicine|May 30, 2018
Chromosomal microarray findings in pregnancies with an isolated pelvic kidneyLena Sagi-Dain, Amihood Singer, Ayala Frumkin, et al.
Journal of Human Genetics|September 19, 2020
Expansion of the GRIA2 phenotypic representation: a novel de novo loss of function mutation in a case with childhood onset schizophreniaAnna Alkelai, Shahar Shohat, Lior Greenbaum, et al.
Pageof 3

Showing results (11-20 of 21) with videos related to

Sort By:
Pageof 3
Cancer Genetics and Cytogenetics|April 22, 2009
Genetic alterations detected by comparative genomic hybridization and recurrence rate in epithelial ovarian carcinomaIlan Bruchim, Ofir Israeli, Salaheddin M Mahmud, et al.
Investigative Ophthalmology & Visual Science|November 24, 2006
Mapping of a gene causing brittle cornea syndrome in Tunisian jews to 16q24Almogit Abu, Moshe Frydman, Dina Marek, et al.
Journal of Assisted Reproduction and Genetics|April 19, 2013
Chromosomal integrity of human preimplantation embryos at different days post fertilizationMichal Dekel-Naftali, Ayala Aviram-Goldring, Talia Litmanovitch, et al.
Neurology. Genetics|June 3, 2021
Chromosomal Microarray Analysis in Pregnancies With Corpus Callosum or Posterior Fossa AnomaliesLior Greenbaum, Idit Maya, Lena Sagi-Dain, et al.
Cancer Genetics and Cytogenetics|September 24, 2004
Genomic analyses of primary and metastatic serous epithelial ovarian cancerOfir Israeli, Walter H Gotlieb, Eitan Friedman, et al.
Journal of Neurosurgery|November 8, 2005
Epidermal growth factor receptor gene amplification and expression in disseminated pediatric low-grade gliomasUri Tabori, Shlomit Rienstein, Yaara Dromi, et al.
Journal of Assisted Reproduction and Genetics|September 28, 2010
Preimplantation genetic haplotyping a new application for diagnosis of translocation carrier's embryos- preliminary observations of two robertsonian translocation carrier familiesJana Shamash, Shlomit Rienstein, Haike Wolf-Reznik, et al.
European Journal of Human Genetics : EJHG|June 21, 2012
Screening of human pluripotent stem cells using CGH and FISH reveals low-grade mosaic aneuploidy and a recurrent amplification of chromosome 1qMichal Dekel-Naftali, Ayala Aviram-Goldring, Talia Litmanovitch, et al.
Journal of Perinatal Medicine|May 30, 2018
Chromosomal microarray findings in pregnancies with an isolated pelvic kidneyLena Sagi-Dain, Amihood Singer, Ayala Frumkin, et al.
Journal of Human Genetics|September 19, 2020
Expansion of the GRIA2 phenotypic representation: a novel de novo loss of function mutation in a case with childhood onset schizophreniaAnna Alkelai, Shahar Shohat, Lior Greenbaum, et al.
Pageof 3