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The New England Journal of Medicine
|
September 7, 2022
Rapid Nanopore Sequencing-Based Screen for Aneuploidy in Reproductive Care
Shan Wei, Alexandre Djandji, Miriam T Lattin, et al.
Journal of Gastrointestinal Oncology
|
May 19, 2025
Claudin 18 immunohistochemistry in cholangiocarcinoma
Niyati Desai, Huaibin M Ko, Michael Lee, et al.
American Journal of Medical Genetics
|
March 14, 2002
Unique case of mosaicism involving two morphologically similar marker chromosomes of different centric origin in a patient with developmental delay
Brynn Levy, Syed M Jalal, Teresa M Dunn, et al.
Annals of Neurology
|
December 23, 2011
Glut1 deficiency syndrome and erythrocyte glucose uptake assay
Hong Yang, Dong Wang, Kristin Engelstad, et al.
Oncotarget
|
May 21, 2016
Genetic landscape of T- and NK-cell post-transplant lymphoproliferative disorders
Elizabeth Margolskee, Vaidehi Jobanputra, Preti Jain, et al.
Science Translational Medicine
|
November 28, 2014
Induced pluripotent stem cells from human revertant keratinocytes for the treatment of epidermolysis bullosa
Noriko Umegaki-Arao, Anna M G Pasmooij, Munenari Itoh, et al.
JCO Precision Oncology
|
February 22, 2023
Integration of a Cross-Ancestry Polygenic Model With Clinical Risk Factors Improves Breast Cancer Risk Stratification
Placede T Tshiaba, Dariusz K Ratman, Jiayi M Sun, et al.
Molecular Cell
|
October 21, 2017
Restoration of Replication Fork Stability in BRCA1- and BRCA2-Deficient Cells by Inactivation of SNF2-Family Fork Remodelers
Angelo Taglialatela, Silvia Alvarez, Giuseppe Leuzzi, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 2, 2012
Tetrasomy 15q26: a distinct syndrome or Shprintzen-Goldberg syndrome phenocopy?
Brynn Levy, David Tegay, Peter Papenhausen, et al.
Stem Cell Research
|
October 30, 2016
Induced pluripotent stem cells (iPSC) created from skin fibroblasts of patients with Prader-Willi syndrome (PWS) retain the molecular signature of PWS
Lisa C Burnett, Charles A LeDuc, Carlos R Sulsona, et al.
Page
of 13
Search research articles
Search
Showing results (71-80 of 122) with videos related to
Sort By:
Page
of 13
The New England Journal of Medicine
|
September 7, 2022
Rapid Nanopore Sequencing-Based Screen for Aneuploidy in Reproductive Care
Shan Wei, Alexandre Djandji, Miriam T Lattin, et al.
Journal of Gastrointestinal Oncology
|
May 19, 2025
Claudin 18 immunohistochemistry in cholangiocarcinoma
Niyati Desai, Huaibin M Ko, Michael Lee, et al.
American Journal of Medical Genetics
|
March 14, 2002
Unique case of mosaicism involving two morphologically similar marker chromosomes of different centric origin in a patient with developmental delay
Brynn Levy, Syed M Jalal, Teresa M Dunn, et al.
Annals of Neurology
|
December 23, 2011
Glut1 deficiency syndrome and erythrocyte glucose uptake assay
Hong Yang, Dong Wang, Kristin Engelstad, et al.
Oncotarget
|
May 21, 2016
Genetic landscape of T- and NK-cell post-transplant lymphoproliferative disorders
Elizabeth Margolskee, Vaidehi Jobanputra, Preti Jain, et al.
Science Translational Medicine
|
November 28, 2014
Induced pluripotent stem cells from human revertant keratinocytes for the treatment of epidermolysis bullosa
Noriko Umegaki-Arao, Anna M G Pasmooij, Munenari Itoh, et al.
JCO Precision Oncology
|
February 22, 2023
Integration of a Cross-Ancestry Polygenic Model With Clinical Risk Factors Improves Breast Cancer Risk Stratification
Placede T Tshiaba, Dariusz K Ratman, Jiayi M Sun, et al.
Molecular Cell
|
October 21, 2017
Restoration of Replication Fork Stability in BRCA1- and BRCA2-Deficient Cells by Inactivation of SNF2-Family Fork Remodelers
Angelo Taglialatela, Silvia Alvarez, Giuseppe Leuzzi, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 2, 2012
Tetrasomy 15q26: a distinct syndrome or Shprintzen-Goldberg syndrome phenocopy?
Brynn Levy, David Tegay, Peter Papenhausen, et al.
Stem Cell Research
|
October 30, 2016
Induced pluripotent stem cells (iPSC) created from skin fibroblasts of patients with Prader-Willi syndrome (PWS) retain the molecular signature of PWS
Lisa C Burnett, Charles A LeDuc, Carlos R Sulsona, et al.
Page
of 13