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Journal of the Association of Genetic Technologists
|
September 4, 2004
Fanconi Anemia: A Decade of Discoveries
Yassmine Akkari, Susan Olson
Genes
|
August 28, 2025
Optical Genome Mapping: A New Tool for Cytogenomic Analysis
Brynn Levy, Rachel D Burnside, Yassmine Akkari
Cold Spring Harbor Molecular Case Studies
|
June 5, 2019
Implementation of cancer next-generation sequencing testing in a community hospital
Yassmine Akkari, Tamara Smith, Jennifer Westfall, et al.
Cancer Genetics
|
July 8, 2022
A novel heptasomy 21 associated with complete loss of heterozygosity and loss of function RUNX1 mutation in acute myeloid leukemia
Fei Yang, Yassmine Akkari, Guang Fan, et al.
Genetics in Medicine Open
|
December 13, 2024
Exploring current challenges in the technologist workforce of clinical genomics laboratories
Yassmine Akkari, Sheila Dobin, Robert G Best, et al.
DNA Repair
|
September 12, 2003
siRNA depletion of BRCA1, but not BRCA2, causes increased genome instability in Fanconi anemia cells
Donald Bruun, Alexandra Folias, Yassmine Akkari, et al.
Human Molecular Genetics
|
September 2, 2005
Fancd2 functions in a double strand break repair pathway that is distinct from non-homologous end joining
Scott Houghtaling, Amy Newell, Yassmine Akkari, et al.
Leukemia
|
November 12, 2021
Recommendations for future extensions to the HGNC gene fusion nomenclature
Alex H Wagner, Yassmine Akkari, Marilyn Li, et al.
Leukemia
|
December 15, 2021
Correction to: Recommendations for future extensions to the HGNC gene fusion nomenclature
Alex H Wagner, Yassmine Akkari, Marilyn Li, et al.
Cancer Research
|
January 25, 2005
Heterozygosity for p53 (Trp53+/-) accelerates epithelial tumor formation in fanconi anemia complementation group D2 (Fancd2) knockout mice
Scott Houghtaling, Laura Granville, Yassmine Akkari, et al.
Page
of 4
Search research articles
Search
Showing results (1-10 of 40) with videos related to
Sort By:
Page
of 4
Journal of the Association of Genetic Technologists
|
September 4, 2004
Fanconi Anemia: A Decade of Discoveries
Yassmine Akkari, Susan Olson
Genes
|
August 28, 2025
Optical Genome Mapping: A New Tool for Cytogenomic Analysis
Brynn Levy, Rachel D Burnside, Yassmine Akkari
Cold Spring Harbor Molecular Case Studies
|
June 5, 2019
Implementation of cancer next-generation sequencing testing in a community hospital
Yassmine Akkari, Tamara Smith, Jennifer Westfall, et al.
Cancer Genetics
|
July 8, 2022
A novel heptasomy 21 associated with complete loss of heterozygosity and loss of function RUNX1 mutation in acute myeloid leukemia
Fei Yang, Yassmine Akkari, Guang Fan, et al.
Genetics in Medicine Open
|
December 13, 2024
Exploring current challenges in the technologist workforce of clinical genomics laboratories
Yassmine Akkari, Sheila Dobin, Robert G Best, et al.
DNA Repair
|
September 12, 2003
siRNA depletion of BRCA1, but not BRCA2, causes increased genome instability in Fanconi anemia cells
Donald Bruun, Alexandra Folias, Yassmine Akkari, et al.
Human Molecular Genetics
|
September 2, 2005
Fancd2 functions in a double strand break repair pathway that is distinct from non-homologous end joining
Scott Houghtaling, Amy Newell, Yassmine Akkari, et al.
Leukemia
|
November 12, 2021
Recommendations for future extensions to the HGNC gene fusion nomenclature
Alex H Wagner, Yassmine Akkari, Marilyn Li, et al.
Leukemia
|
December 15, 2021
Correction to: Recommendations for future extensions to the HGNC gene fusion nomenclature
Alex H Wagner, Yassmine Akkari, Marilyn Li, et al.
Cancer Research
|
January 25, 2005
Heterozygosity for p53 (Trp53+/-) accelerates epithelial tumor formation in fanconi anemia complementation group D2 (Fancd2) knockout mice
Scott Houghtaling, Laura Granville, Yassmine Akkari, et al.
Page
of 4