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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 adenocarcinoma
Jorge 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 Mapping
Rashmi 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 Diagnosis
Liesbeth Vossaert, Qun Wang, Roseen Salman, et al.
Cancer Genetics
|
October 12, 2015
A multicenter, cross-platform clinical validation study of cancer cytogenomic arrays
Marilyn 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 overgrowth
Gina 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 study
Slavé Petrovski, Vimla Aggarwal, Jessica L Giordano, et al.
Blood
|
February 15, 2022
Guiding the global evolution of cytogenetic testing for hematologic malignancies
Yassmine 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 disease
Zuhair 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 stillbirth
Uma 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 diagnosis
Ronald J Wapner, Christa Lese Martin, Brynn Levy, et al.
Page
of 13
Search research articles
Search
Showing results (101-110 of 122) with videos related to
Sort By:
Page
of 13
International Journal of Cancer
|
April 20, 2019
High-resolution genomic alterations in Barrett's metaplasia of patients who progress to esophageal dysplasia and adenocarcinoma
Jorge 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 Mapping
Rashmi 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 Diagnosis
Liesbeth Vossaert, Qun Wang, Roseen Salman, et al.
Cancer Genetics
|
October 12, 2015
A multicenter, cross-platform clinical validation study of cancer cytogenomic arrays
Marilyn 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 overgrowth
Gina 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 study
Slavé Petrovski, Vimla Aggarwal, Jessica L Giordano, et al.
Blood
|
February 15, 2022
Guiding the global evolution of cytogenetic testing for hematologic malignancies
Yassmine 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 disease
Zuhair 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 stillbirth
Uma 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 diagnosis
Ronald J Wapner, Christa Lese Martin, Brynn Levy, et al.
Page
of 13