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Yuval Yaron

Showing results (71-80 of 122) with videos related to

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Prenatal Diagnosis|October 11, 2022
Upgrading an intronic TMEM67 variant of unknown significance to likely pathogenic through RNA studies and community data sharingAlina Kurolap, Adi Mory, Sharon Simchoni, et al.
Cancer|August 14, 2002
Clinical and screening implications of the I1307K adenomatous polyposis coli gene variant in Israeli Ashkenazi Jews with familial colorectal neoplasia. Evidence for a founder effectPaul Rozen, Tova Naiman, Hana Strul, et al.
Fetal Diagnosis and Therapy|April 25, 2003
Demographic factors for utilization of invasive genetic testing after multifetal pregnancy reductionCarol L Baker, Baruch Feldman, Alex G Shalhoub, et al.
Journal of Child Neurology|March 27, 2002
Rett syndrome: clinical manifestations in males with MECP2 mutationsBruria Ben Zeev, Yuval Yaron, N Carolyn Schanen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 31, 2014
Ethnic effect on FMR1 carrier rate and AGG repeat interruptions among Ashkenazi womenKarin Weiss, Avi Orr-Urtreger, Idit Kaplan Ber, et al.
Prenatal Diagnosis|December 15, 2005
Preimplantation genetic diagnosis (PGD) for Duchenne muscular dystrophy (DMD) by triplex-nested PCRMira Malcov, Dalit Ben-Yosef, Tamar Schwartz, et al.
Journal of Medical Genetics|December 18, 2012
Paternal deletion of the 11p15.5 centromeric-imprinting control region is associated with alteration of imprinted gene expression and recurrent severe intrauterine growth restrictionAgostina De Crescenzo, Angela Sparago, Flavia Cerrato, et al.
In Vitro Cellular & Developmental Biology. Animal|February 27, 2010
Human embryonic stem cells carrying mutations for severe genetic disordersTsvia Frumkin, Mira Malcov, Michael Telias, et al.
Prenatal Diagnosis|March 11, 2014
Microscopic chromosome Xp distal deletions--a challenging issue in prenatal genetic counselingRivka Sukenik-Halevy, Adi Reches, Anat Bar-Shira, et al.
Cancer Research|December 4, 2002
Multiple genes in human 20q13 chromosomal region are involved in an advanced prostate cancer xenograftAnat Bar-Shira, Jehonathan H Pinthus, Uri Rozovsky, et al.
Pageof 13

Showing results (71-80 of 122) with videos related to

Sort By:
Pageof 13
Prenatal Diagnosis|October 11, 2022
Upgrading an intronic TMEM67 variant of unknown significance to likely pathogenic through RNA studies and community data sharingAlina Kurolap, Adi Mory, Sharon Simchoni, et al.
Cancer|August 14, 2002
Clinical and screening implications of the I1307K adenomatous polyposis coli gene variant in Israeli Ashkenazi Jews with familial colorectal neoplasia. Evidence for a founder effectPaul Rozen, Tova Naiman, Hana Strul, et al.
Fetal Diagnosis and Therapy|April 25, 2003
Demographic factors for utilization of invasive genetic testing after multifetal pregnancy reductionCarol L Baker, Baruch Feldman, Alex G Shalhoub, et al.
Journal of Child Neurology|March 27, 2002
Rett syndrome: clinical manifestations in males with MECP2 mutationsBruria Ben Zeev, Yuval Yaron, N Carolyn Schanen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 31, 2014
Ethnic effect on FMR1 carrier rate and AGG repeat interruptions among Ashkenazi womenKarin Weiss, Avi Orr-Urtreger, Idit Kaplan Ber, et al.
Prenatal Diagnosis|December 15, 2005
Preimplantation genetic diagnosis (PGD) for Duchenne muscular dystrophy (DMD) by triplex-nested PCRMira Malcov, Dalit Ben-Yosef, Tamar Schwartz, et al.
Journal of Medical Genetics|December 18, 2012
Paternal deletion of the 11p15.5 centromeric-imprinting control region is associated with alteration of imprinted gene expression and recurrent severe intrauterine growth restrictionAgostina De Crescenzo, Angela Sparago, Flavia Cerrato, et al.
In Vitro Cellular & Developmental Biology. Animal|February 27, 2010
Human embryonic stem cells carrying mutations for severe genetic disordersTsvia Frumkin, Mira Malcov, Michael Telias, et al.
Prenatal Diagnosis|March 11, 2014
Microscopic chromosome Xp distal deletions--a challenging issue in prenatal genetic counselingRivka Sukenik-Halevy, Adi Reches, Anat Bar-Shira, et al.
Cancer Research|December 4, 2002
Multiple genes in human 20q13 chromosomal region are involved in an advanced prostate cancer xenograftAnat Bar-Shira, Jehonathan H Pinthus, Uri Rozovsky, et al.
Pageof 13