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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 families
Jana Shamash, Shlomit Rienstein, Haike Wolf-Reznik, et al.
Chembiochem : a European Journal of Chemical Biology
|
May 2, 2015
A Recombinant Collagen-mRNA Platform for Controllable Protein Synthesis
Liping Sun, Yunjing Xiong, Anat Bashan, et al.
Human Genetics
|
March 20, 2013
Whole exome sequencing in dominant cataract identifies a new causative factor, CRYBA2, and a variety of novel alleles in known genes
Linda M Reis, Rebecca C Tyler, Sanaa Muheisen, et al.
Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences
|
March 6, 2025
Ribosomes: from conserved origin to functional/medical mobility and heterogeneity
Andre Rivalta, Disha-Gajanan Hiregange, Tanaya Bose, et al.
Prenatal Diagnosis
|
February 28, 2012
Carrier state for the nebulin exon 55 deletion and abnormal prenatal ultrasound findings as potential signs of nemaline myopathy
Hagith Yonath, Haike Reznik-Wolf, Michal Berkenstadt, et al.
Obstetrics and Gynecology
|
November 7, 2018
Chromosomal Microarray Analysis Results From Pregnancies With Various Ultrasonographic Anomalies
Lena Sagi-Dain, Idit Maya, Adi Reches, et al.
International Journal of Cardiology
|
June 14, 2020
Reduction in Filamin C transcript is associated with arrhythmogenic cardiomyopathy in Ashkenazi Jews
Shimrit Oz, Hagith Yonath, Leonid Visochyk, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
April 17, 2008
Microduplications of 22q11.2 are frequently inherited and are associated with variable phenotypes
Zhishuo Ou, Jonathan S Berg, Hagith Yonath, 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 study
Rachel Michaelson-Cohen, Liat Sheelo Salzer, Dana Brabbing-Goldstein, et al.
Journal of the Neurological Sciences
|
July 5, 2024
The yield of genetic workup for middle-aged and elderly patients with neurological disorders in a real-world setting
Noga Lempel, Shahar Shelly, Odelia Chorin, et al.
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of 4
Search research articles
Search
Showing results (21-30 of 36) with videos related to
Sort By:
Page
of 4
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 families
Jana Shamash, Shlomit Rienstein, Haike Wolf-Reznik, et al.
Chembiochem : a European Journal of Chemical Biology
|
May 2, 2015
A Recombinant Collagen-mRNA Platform for Controllable Protein Synthesis
Liping Sun, Yunjing Xiong, Anat Bashan, et al.
Human Genetics
|
March 20, 2013
Whole exome sequencing in dominant cataract identifies a new causative factor, CRYBA2, and a variety of novel alleles in known genes
Linda M Reis, Rebecca C Tyler, Sanaa Muheisen, et al.
Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences
|
March 6, 2025
Ribosomes: from conserved origin to functional/medical mobility and heterogeneity
Andre Rivalta, Disha-Gajanan Hiregange, Tanaya Bose, et al.
Prenatal Diagnosis
|
February 28, 2012
Carrier state for the nebulin exon 55 deletion and abnormal prenatal ultrasound findings as potential signs of nemaline myopathy
Hagith Yonath, Haike Reznik-Wolf, Michal Berkenstadt, et al.
Obstetrics and Gynecology
|
November 7, 2018
Chromosomal Microarray Analysis Results From Pregnancies With Various Ultrasonographic Anomalies
Lena Sagi-Dain, Idit Maya, Adi Reches, et al.
International Journal of Cardiology
|
June 14, 2020
Reduction in Filamin C transcript is associated with arrhythmogenic cardiomyopathy in Ashkenazi Jews
Shimrit Oz, Hagith Yonath, Leonid Visochyk, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
April 17, 2008
Microduplications of 22q11.2 are frequently inherited and are associated with variable phenotypes
Zhishuo Ou, Jonathan S Berg, Hagith Yonath, 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 study
Rachel Michaelson-Cohen, Liat Sheelo Salzer, Dana Brabbing-Goldstein, et al.
Journal of the Neurological Sciences
|
July 5, 2024
The yield of genetic workup for middle-aged and elderly patients with neurological disorders in a real-world setting
Noga Lempel, Shahar Shelly, Odelia Chorin, et al.
Page
of 4