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Brynn Levy

Showing results (101-110 of 122) with videos related to

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International Journal of Cancer|April 20, 2019
High-resolution genomic alterations in Barrett's metaplasia of patients who progress to esophageal dysplasia and adenocarcinomaJorge L Sepulveda, Elena V Komissarova, Sarawut Kongkarnka, et al.
American Journal of Hematology|April 30, 2025
Integration of Optical Genome Mapping in the Cytogenomic and Molecular Work-Up of Hematological Malignancies: Expert Recommendations From the International Consortium for Optical Genome MappingRashmi Kanagal-Shamanna, Anna Puiggros, Isabel Granada, et al.
American Journal of Human Genetics|December 2, 2019
Validation Studies for Single Circulating Trophoblast Genetic Testing as a Form of Noninvasive Prenatal DiagnosisLiesbeth Vossaert, Qun Wang, Roseen Salman, et al.
Cancer Genetics|October 12, 2015
A multicenter, cross-platform clinical validation study of cancer cytogenomic arraysMarilyn M Li, Federico A Monzon, Jaclyn A Biegel, et al.
Plos Genetics|May 17, 2014
Mutations in the cholesterol transporter gene ABCA5 are associated with excessive hair overgrowthGina M DeStefano, Mazen Kurban, Kwame Anyane-Yeboa, et al.
Lancet (London, England)|February 5, 2019
Whole-exome sequencing in the evaluation of fetal structural anomalies: a prospective cohort studySlavé Petrovski, Vimla Aggarwal, Jessica L Giordano, et al.
Blood|February 15, 2022
Guiding the global evolution of cytogenetic testing for hematologic malignanciesYassmine M N Akkari, Linda B Baughn, Adrian M Dubuc, et al.
Molecular Cytogenetics|February 9, 2018
Identification of novel genomic imbalances in Saudi patients with congenital heart diseaseZuhair N Al-Hassnan, Waad Albawardi, Faten Almutairi, et al.
The New England Journal of Medicine|December 11, 2012
Karyotype versus microarray testing for genetic abnormalities after stillbirthUma M Reddy, Grier P Page, George R Saade, et al.
The New England Journal of Medicine|December 11, 2012
Chromosomal microarray versus karyotyping for prenatal diagnosisRonald J Wapner, Christa Lese Martin, Brynn Levy, et al.
Pageof 13

Showing results (101-110 of 122) with videos related to

Sort By:
Pageof 13
International Journal of Cancer|April 20, 2019
High-resolution genomic alterations in Barrett's metaplasia of patients who progress to esophageal dysplasia and adenocarcinomaJorge L Sepulveda, Elena V Komissarova, Sarawut Kongkarnka, et al.
American Journal of Hematology|April 30, 2025
Integration of Optical Genome Mapping in the Cytogenomic and Molecular Work-Up of Hematological Malignancies: Expert Recommendations From the International Consortium for Optical Genome MappingRashmi Kanagal-Shamanna, Anna Puiggros, Isabel Granada, et al.
American Journal of Human Genetics|December 2, 2019
Validation Studies for Single Circulating Trophoblast Genetic Testing as a Form of Noninvasive Prenatal DiagnosisLiesbeth Vossaert, Qun Wang, Roseen Salman, et al.
Cancer Genetics|October 12, 2015
A multicenter, cross-platform clinical validation study of cancer cytogenomic arraysMarilyn M Li, Federico A Monzon, Jaclyn A Biegel, et al.
Plos Genetics|May 17, 2014
Mutations in the cholesterol transporter gene ABCA5 are associated with excessive hair overgrowthGina M DeStefano, Mazen Kurban, Kwame Anyane-Yeboa, et al.
Lancet (London, England)|February 5, 2019
Whole-exome sequencing in the evaluation of fetal structural anomalies: a prospective cohort studySlavé Petrovski, Vimla Aggarwal, Jessica L Giordano, et al.
Blood|February 15, 2022
Guiding the global evolution of cytogenetic testing for hematologic malignanciesYassmine M N Akkari, Linda B Baughn, Adrian M Dubuc, et al.
Molecular Cytogenetics|February 9, 2018
Identification of novel genomic imbalances in Saudi patients with congenital heart diseaseZuhair N Al-Hassnan, Waad Albawardi, Faten Almutairi, et al.
The New England Journal of Medicine|December 11, 2012
Karyotype versus microarray testing for genetic abnormalities after stillbirthUma M Reddy, Grier P Page, George R Saade, et al.
The New England Journal of Medicine|December 11, 2012
Chromosomal microarray versus karyotyping for prenatal diagnosisRonald J Wapner, Christa Lese Martin, Brynn Levy, et al.
Pageof 13