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Genes
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January 8, 2025
Conventional Cytogenetic Analysis of Solid Tumor Abnormalities: A 25-Year Review of Proficiency Test Results from the College of American Pathologists/American College of Medical Genetics and Genomics Cytogenetics Committee
Rachel K Vanderscheldon, William R Sukov, Juli-Anne Gardner, et al.
Cancer Research
|
November 17, 2007
Deregulated overexpression of hCdt1 and hCdc6 promotes malignant behavior
Michalis Liontos, Marilena Koutsami, Maria Sideridou, et al.
Genetics in Medicine Open
|
December 9, 2025
Childhood outcomes of fetal genomic copy-number variants: The prenatal microarray cohort study
Jacqui McCoy, Cecilia Pynaker, Sharon Lewis, et al.
Oncotarget
|
June 2, 2016
The genetic landscape of dural marginal zone lymphomas
Karthik A Ganapathi, Vaidehi Jobanputra, Fabio Iwamoto, et al.
Prenatal Diagnosis
|
October 26, 2018
Reliable detection of subchromosomal deletions and duplications using cell-based noninvasive prenatal testing
Liesbeth Vossaert, Qun Wang, Roseen Salman, et al.
Archives of Pathology & Laboratory Medicine
|
June 5, 2024
Conventional Cytogenetic Analysis of Constitutional Abnormalities: A 20-Year Review of Proficiency Test Results From the College of American Pathologists/American College of Medical Genetics and Genomics Cytogenetics Committee
Brittney Boles, Juli-Anne Gardner, Catherine W Rehder, et al.
Blood Advances
|
November 23, 2022
Optical genome mapping in acute myeloid leukemia: a multicenter evaluation
Brynn Levy, Linda B Baughn, Yassmine Akkari, et al.
American Journal of Hematology
|
January 2, 2024
A framework for the clinical implementation of optical genome mapping in hematologic malignancies
Brynn Levy, Rashmi Kanagal-Shamanna, Nikhil S Sahajpal, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
April 23, 2013
Position effect on FGF13 associated with X-linked congenital generalized hypertrichosis
Gina M DeStefano, Katherine A Fantauzzo, Lynn Petukhova, et al.
American Journal of Obstetrics and Gynecology
|
December 6, 2014
Expanding the scope of noninvasive prenatal testing: detection of fetal microdeletion syndromes
Ronald J Wapner, Joshua E Babiarz, Brynn Levy, et al.
Page
of 13
Search research articles
Search
Showing results (91-100 of 122) with videos related to
Sort By:
Page
of 13
Genes
|
January 8, 2025
Conventional Cytogenetic Analysis of Solid Tumor Abnormalities: A 25-Year Review of Proficiency Test Results from the College of American Pathologists/American College of Medical Genetics and Genomics Cytogenetics Committee
Rachel K Vanderscheldon, William R Sukov, Juli-Anne Gardner, et al.
Cancer Research
|
November 17, 2007
Deregulated overexpression of hCdt1 and hCdc6 promotes malignant behavior
Michalis Liontos, Marilena Koutsami, Maria Sideridou, et al.
Genetics in Medicine Open
|
December 9, 2025
Childhood outcomes of fetal genomic copy-number variants: The prenatal microarray cohort study
Jacqui McCoy, Cecilia Pynaker, Sharon Lewis, et al.
Oncotarget
|
June 2, 2016
The genetic landscape of dural marginal zone lymphomas
Karthik A Ganapathi, Vaidehi Jobanputra, Fabio Iwamoto, et al.
Prenatal Diagnosis
|
October 26, 2018
Reliable detection of subchromosomal deletions and duplications using cell-based noninvasive prenatal testing
Liesbeth Vossaert, Qun Wang, Roseen Salman, et al.
Archives of Pathology & Laboratory Medicine
|
June 5, 2024
Conventional Cytogenetic Analysis of Constitutional Abnormalities: A 20-Year Review of Proficiency Test Results From the College of American Pathologists/American College of Medical Genetics and Genomics Cytogenetics Committee
Brittney Boles, Juli-Anne Gardner, Catherine W Rehder, et al.
Blood Advances
|
November 23, 2022
Optical genome mapping in acute myeloid leukemia: a multicenter evaluation
Brynn Levy, Linda B Baughn, Yassmine Akkari, et al.
American Journal of Hematology
|
January 2, 2024
A framework for the clinical implementation of optical genome mapping in hematologic malignancies
Brynn Levy, Rashmi Kanagal-Shamanna, Nikhil S Sahajpal, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
April 23, 2013
Position effect on FGF13 associated with X-linked congenital generalized hypertrichosis
Gina M DeStefano, Katherine A Fantauzzo, Lynn Petukhova, et al.
American Journal of Obstetrics and Gynecology
|
December 6, 2014
Expanding the scope of noninvasive prenatal testing: detection of fetal microdeletion syndromes
Ronald J Wapner, Joshua E Babiarz, Brynn Levy, et al.
Page
of 13