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Hagit Daum

Showing results (31-40 of 41) with videos related to

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Clinical Genetics|May 22, 2025
RNA Analysis Enables Resolution and Reclassification of Reportedly Benign Synonymous VariantsAdina Fuchs, Inbar Kobal, Dov Popper, et al.
Breast Cancer Research and Treatment|March 1, 2013
Tumor STAT3 tyrosine phosphorylation status, as a predictor of benefit from adjuvant chemotherapy for breast cancerAmir Sonnenblick, Beatrice Uziely, Hovav Nechushtan, et al.
Fetal Diagnosis and Therapy|December 22, 2020
The Yield of Chromosomal Microarray in Pregnancies Complicated with Fetal Growth Restriction Can Be Predicted According to Clinical ParametersKeren Tzadikevitch Geffen, Amihood Singer, Idit Maya, et al.
European Journal of Human Genetics : EJHG|February 15, 2020
Smith-Lemli-Opitz syndrome: what is the actual risk for couples carriers of the DHCR7:c.964-1G>C variant?Hagit Daum, Vardiella Meiner, Rachel Michaelson-Cohen, et al.
Archives of Gynecology and Obstetrics|August 8, 2020
Chromosomal microarray should be performed for cases of fetal short long bones detected prenatallyKeren Tzadikevitch Geffen, Amihood Singer, Idit Maya, et al.
Hormone Research in Paediatrics|November 22, 2017
Failure to Thrive in the Context of Carney ComplexAmit Tirosh, Adi Auerbach, Belen Bonella, et al.
Clinical Genetics|September 27, 2025
High Concordance of Copy Number Variants Detected by Chromosomal Microarray and Exome Sequencing in Clinical DiagnosticsRivka Birnbaum, Maya Slovik, Shamir Zenvirt, et al.
European Journal of Human Genetics : EJHG|September 7, 2022
Exome sequencing for structurally normal fetuses-yields and ethical issuesHagit Daum, Tamar Harel, Talya Millo, et al.
Prenatal Diagnosis|February 14, 2024
Exploring the factors affecting classification and reporting of uncertain prenatal microarray findings, using a "virtual fetus" model-a pilot studyRachel Michaelson-Cohen, Liat Sheelo Salzer, Dana Brabbing-Goldstein, et al.
Blood|September 2, 2018
<i>GNE</i> variants causing autosomal recessive macrothrombocytopenia without associated muscle wastingShoshana Revel-Vilk, Ela Shai, Ernest Turro, et al.
Pageof 5

Showing results (31-40 of 41) with videos related to

Sort By:
Pageof 5
Clinical Genetics|May 22, 2025
RNA Analysis Enables Resolution and Reclassification of Reportedly Benign Synonymous VariantsAdina Fuchs, Inbar Kobal, Dov Popper, et al.
Breast Cancer Research and Treatment|March 1, 2013
Tumor STAT3 tyrosine phosphorylation status, as a predictor of benefit from adjuvant chemotherapy for breast cancerAmir Sonnenblick, Beatrice Uziely, Hovav Nechushtan, et al.
Fetal Diagnosis and Therapy|December 22, 2020
The Yield of Chromosomal Microarray in Pregnancies Complicated with Fetal Growth Restriction Can Be Predicted According to Clinical ParametersKeren Tzadikevitch Geffen, Amihood Singer, Idit Maya, et al.
European Journal of Human Genetics : EJHG|February 15, 2020
Smith-Lemli-Opitz syndrome: what is the actual risk for couples carriers of the DHCR7:c.964-1G>C variant?Hagit Daum, Vardiella Meiner, Rachel Michaelson-Cohen, et al.
Archives of Gynecology and Obstetrics|August 8, 2020
Chromosomal microarray should be performed for cases of fetal short long bones detected prenatallyKeren Tzadikevitch Geffen, Amihood Singer, Idit Maya, et al.
Hormone Research in Paediatrics|November 22, 2017
Failure to Thrive in the Context of Carney ComplexAmit Tirosh, Adi Auerbach, Belen Bonella, et al.
Clinical Genetics|September 27, 2025
High Concordance of Copy Number Variants Detected by Chromosomal Microarray and Exome Sequencing in Clinical DiagnosticsRivka Birnbaum, Maya Slovik, Shamir Zenvirt, et al.
European Journal of Human Genetics : EJHG|September 7, 2022
Exome sequencing for structurally normal fetuses-yields and ethical issuesHagit Daum, Tamar Harel, Talya Millo, et al.
Prenatal Diagnosis|February 14, 2024
Exploring the factors affecting classification and reporting of uncertain prenatal microarray findings, using a "virtual fetus" model-a pilot studyRachel Michaelson-Cohen, Liat Sheelo Salzer, Dana Brabbing-Goldstein, et al.
Blood|September 2, 2018
<i>GNE</i> variants causing autosomal recessive macrothrombocytopenia without associated muscle wastingShoshana Revel-Vilk, Ela Shai, Ernest Turro, et al.
Pageof 5