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Idit Maya

Showing results (31-40 of 67) with videos related to

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Archives of Gynecology and Obstetrics|March 18, 2024
Chromosomal microarray testing yield in 829 cases of microcephaly: a clinical characteristics-based analysis for prenatal and postnatal casesRivka Sukenik-Halevy, Nir Mevorach, Lina Basel-Salmon, 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.
European Journal of Medical Genetics|July 24, 2020
Based on a cohort of 52,879 microarrays, recurrent intragenic FBN2 deletion encompassing exons 1-8 does not cause Beals syndromeIdit Maya, Sarit Kahana, Ifaat Agmon-Fishman, et al.
American Journal of Perinatology|April 30, 2024
The Diagnostic Yield of Chromosomal Microarray Analysis in Third-Trimester Fetal AbnormalitiesEyal Elron, Idit Maya, Noa Shefer-Averbuch, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 25, 2019
Chromosomal microarray vs. NIPS: analysis of 5541 low-risk pregnanciesLena Sagi-Dain, Lital Cohen Vig, Sarit Kahana, et al.
Journal of Clinical Medicine|August 16, 2020
Should We Report 15q11.2 BP1-BP2 Deletions and Duplications in the Prenatal Setting?Idit Maya, Sharon Perlman, Mordechai Shohat, et al.
Journal of Perinatal Medicine|July 29, 2020
The yield of chromosomal microarray testing for cases of abnormal fetal head circumferenceYael Pasternak, Amihood Singer, Idit Maya, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology|January 26, 2018
Isolated fetal horseshoe kidney does not seem to increase the risk for abnormal chromosomal microarray resultsLena Sagi-Dain, Idit Maya, Tzipora Falik-Zaccai, et al.
American Journal of Obstetrics and Gynecology|November 11, 2021
Residual risk for clinically significant copy number variants in low-risk pregnancies, following exclusion of noninvasive prenatal screening-detectable findingsIdit Maya, Liat Salzer Sheelo, Dana Brabbing-Goldstein, et al.
Obstetrics and Gynecology|May 16, 2022
Chromosomal Microarray Analysis Compared With Noninvasive Prenatal Testing in Pregnancies With Abnormal Maternal Serum ScreeningLena Sagi-Dain, Liat Salzer Sheelo, Dana Brabbing-Goldstein, et al.
Pageof 7

Showing results (31-40 of 67) with videos related to

Sort By:
Pageof 7
Archives of Gynecology and Obstetrics|March 18, 2024
Chromosomal microarray testing yield in 829 cases of microcephaly: a clinical characteristics-based analysis for prenatal and postnatal casesRivka Sukenik-Halevy, Nir Mevorach, Lina Basel-Salmon, 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.
European Journal of Medical Genetics|July 24, 2020
Based on a cohort of 52,879 microarrays, recurrent intragenic FBN2 deletion encompassing exons 1-8 does not cause Beals syndromeIdit Maya, Sarit Kahana, Ifaat Agmon-Fishman, et al.
American Journal of Perinatology|April 30, 2024
The Diagnostic Yield of Chromosomal Microarray Analysis in Third-Trimester Fetal AbnormalitiesEyal Elron, Idit Maya, Noa Shefer-Averbuch, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 25, 2019
Chromosomal microarray vs. NIPS: analysis of 5541 low-risk pregnanciesLena Sagi-Dain, Lital Cohen Vig, Sarit Kahana, et al.
Journal of Clinical Medicine|August 16, 2020
Should We Report 15q11.2 BP1-BP2 Deletions and Duplications in the Prenatal Setting?Idit Maya, Sharon Perlman, Mordechai Shohat, et al.
Journal of Perinatal Medicine|July 29, 2020
The yield of chromosomal microarray testing for cases of abnormal fetal head circumferenceYael Pasternak, Amihood Singer, Idit Maya, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology|January 26, 2018
Isolated fetal horseshoe kidney does not seem to increase the risk for abnormal chromosomal microarray resultsLena Sagi-Dain, Idit Maya, Tzipora Falik-Zaccai, et al.
American Journal of Obstetrics and Gynecology|November 11, 2021
Residual risk for clinically significant copy number variants in low-risk pregnancies, following exclusion of noninvasive prenatal screening-detectable findingsIdit Maya, Liat Salzer Sheelo, Dana Brabbing-Goldstein, et al.
Obstetrics and Gynecology|May 16, 2022
Chromosomal Microarray Analysis Compared With Noninvasive Prenatal Testing in Pregnancies With Abnormal Maternal Serum ScreeningLena Sagi-Dain, Liat Salzer Sheelo, Dana Brabbing-Goldstein, et al.
Pageof 7