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Yuval Yaron

Showing results (51-60 of 122) with videos related to

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Genetic Testing|July 30, 2003
Screening for familial dysautonomia in Israel: evidence for higher carrier rate among Polish Ashkenazi JewsOfer Lehavi, Orna Aizenstein, Dani Bercovich, et al.
Fertility and Sterility|December 27, 2008
Elucidation of abnormal fertilization by single-cell analysis with fluorescence in situ hybridization and polymorphic marker analysisMira Malcov, Tsvia Frumkin, Tamar Shwartz, et al.
Fetal Diagnosis and Therapy|October 5, 2017
Parental Origin of the Retained X Chromosome in Monosomy X Miscarriages and Ongoing PregnanciesMaribel Grande, Iosifina Stergiotou, Montse Pauta, et al.
Prenatal Diagnosis|April 8, 2022
Non-immune hydrops fetalis caused by PIEZO1 compound heterozygous deletions detected only by exome sequencingSivan Reytan, Noa Zunz Henig, Yoav Yinon, et al.
Prenatal Diagnosis|January 21, 2003
The clinical application of spectral karyotyping (SKY) in the analysis of prenatally diagnosed extra structurally abnormal chromosomes (ESACs)Yuval Yaron, Erez Carmon, Myriam Goldstein, et al.
Fetal Diagnosis and Therapy|October 24, 2002
Spontaneous abortions in couples declining multifetal pregnancy reductionMark I Evans, Ronald J Wapner, Melissa A Ayoub, et al.
Cancer Genetics and Cytogenetics|October 12, 2004
Cytogenetic analysis of three variants of clival chordomaZiv Gil, Dan M Fliss, Nadia Voskoboinik, et al.
Fetal Diagnosis and Therapy|October 10, 2009
Loeys-Dietz syndrome in pregnancy: a case description and report of a novel mutationGuy Gutman, Hagit N Baris, Raphael Hirsch, et al.
Prenatal Diagnosis|October 5, 2024
Prenatal Diagnosis of a KIDINS220 De Novo Heterozygous Variant in a Fetus With a Complex CNS AnomalyHadas Miremberg, Roee Birnbaum, Dorin Trigubov, et al.
Cancer Genetics and Cytogenetics|August 26, 2003
Two novel translocations, t(2;4)(q35;q31) and t(X;12)(q22;q24), as the only karyotypic abnormalities in a malignant peripheral nerve sheath tumor of the skull baseZiv Gil, Dan M Fliss, Nadia Voskoboimik, et al.
Pageof 13

Showing results (51-60 of 122) with videos related to

Sort By:
Pageof 13
Genetic Testing|July 30, 2003
Screening for familial dysautonomia in Israel: evidence for higher carrier rate among Polish Ashkenazi JewsOfer Lehavi, Orna Aizenstein, Dani Bercovich, et al.
Fertility and Sterility|December 27, 2008
Elucidation of abnormal fertilization by single-cell analysis with fluorescence in situ hybridization and polymorphic marker analysisMira Malcov, Tsvia Frumkin, Tamar Shwartz, et al.
Fetal Diagnosis and Therapy|October 5, 2017
Parental Origin of the Retained X Chromosome in Monosomy X Miscarriages and Ongoing PregnanciesMaribel Grande, Iosifina Stergiotou, Montse Pauta, et al.
Prenatal Diagnosis|April 8, 2022
Non-immune hydrops fetalis caused by PIEZO1 compound heterozygous deletions detected only by exome sequencingSivan Reytan, Noa Zunz Henig, Yoav Yinon, et al.
Prenatal Diagnosis|January 21, 2003
The clinical application of spectral karyotyping (SKY) in the analysis of prenatally diagnosed extra structurally abnormal chromosomes (ESACs)Yuval Yaron, Erez Carmon, Myriam Goldstein, et al.
Fetal Diagnosis and Therapy|October 24, 2002
Spontaneous abortions in couples declining multifetal pregnancy reductionMark I Evans, Ronald J Wapner, Melissa A Ayoub, et al.
Cancer Genetics and Cytogenetics|October 12, 2004
Cytogenetic analysis of three variants of clival chordomaZiv Gil, Dan M Fliss, Nadia Voskoboinik, et al.
Fetal Diagnosis and Therapy|October 10, 2009
Loeys-Dietz syndrome in pregnancy: a case description and report of a novel mutationGuy Gutman, Hagit N Baris, Raphael Hirsch, et al.
Prenatal Diagnosis|October 5, 2024
Prenatal Diagnosis of a KIDINS220 De Novo Heterozygous Variant in a Fetus With a Complex CNS AnomalyHadas Miremberg, Roee Birnbaum, Dorin Trigubov, et al.
Cancer Genetics and Cytogenetics|August 26, 2003
Two novel translocations, t(2;4)(q35;q31) and t(X;12)(q22;q24), as the only karyotypic abnormalities in a malignant peripheral nerve sheath tumor of the skull baseZiv Gil, Dan M Fliss, Nadia Voskoboimik, et al.
Pageof 13