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Athena M Cherry

Showing results (21-30 of 58) with videos related to

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American Journal of Medical Genetics. Part A|June 9, 2005
Terminal deletion of 6p results in a recognizable phenotypeRuth J Lin, Athena M Cherry, Kelly C Chen, et al.
Pediatric Blood & Cancer|October 7, 2004
Epstein-Barr virus-associated peripheral T-cell lymphoma and hemophagocytic syndrome arising after liver transplantation: case report and review of the literatureTracy I George, Michael Jeng, William Berquist, et al.
Genes, Chromosomes & Cancer|July 22, 2006
Identification of novel Runx1 (AML1) translocation partner genes SH3D19, YTHDf2, and ZNF687 in acute myeloid leukemiaTuDung T Nguyen, Lisa N Ma, Marilyn L Slovak, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 29, 2016
Section E6.1-6.4 of the ACMG technical standards and guidelines: chromosome studies of neoplastic blood and bone marrow-acquired chromosomal abnormalitiesFady M Mikhail, Nyla A Heerema, Kathleen W Rao, et al.
Human Immunology|April 6, 2011
Short tandem repeat and human leukocyte antigen mutations or losses confound engraftment and typing analysis in hematopoietic stem cell transplantsShalini Pereira, Tamara Vayntrub, Debra D Hiraki, et al.
The Journal of Molecular Diagnostics : JMD|July 29, 2005
Low-grade B-Cell lymphomas with plasmacytic differentiation lack PAX5 gene rearrangementsTracy I George, Joanna E Wrede, Charles D Bangs, et al.
American Journal of Clinical Pathology|September 19, 2013
Hidden mastocytosis in acute myeloid leukemia with t(8;21)(q22;q22)Ryan C Johnson, Natasha M Savage, Tsoyu Chiang, et al.
Acta Neuropathologica|July 21, 2007
Gliosarcoma with melanocytic differentiationMohanpal S Dulai, Gregory S Moes, Anita L Briley, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 26, 2013
ACMG Policy Statement. Risk categorization for oversight of laboratory-developed tests for inherited conditionsKristin G Monaghan, Judith Benkendorf, Athena M Cherry, et al.
Pediatrics|August 3, 2004
Terminal 22q deletion syndrome: a newly recognized cause of speech and language disability in the autism spectrumMelanie A Manning, Suzanne B Cassidy, Carol Clericuzio, et al.
Pageof 6

Showing results (21-30 of 58) with videos related to

Sort By:
Pageof 6
American Journal of Medical Genetics. Part A|June 9, 2005
Terminal deletion of 6p results in a recognizable phenotypeRuth J Lin, Athena M Cherry, Kelly C Chen, et al.
Pediatric Blood & Cancer|October 7, 2004
Epstein-Barr virus-associated peripheral T-cell lymphoma and hemophagocytic syndrome arising after liver transplantation: case report and review of the literatureTracy I George, Michael Jeng, William Berquist, et al.
Genes, Chromosomes & Cancer|July 22, 2006
Identification of novel Runx1 (AML1) translocation partner genes SH3D19, YTHDf2, and ZNF687 in acute myeloid leukemiaTuDung T Nguyen, Lisa N Ma, Marilyn L Slovak, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 29, 2016
Section E6.1-6.4 of the ACMG technical standards and guidelines: chromosome studies of neoplastic blood and bone marrow-acquired chromosomal abnormalitiesFady M Mikhail, Nyla A Heerema, Kathleen W Rao, et al.
Human Immunology|April 6, 2011
Short tandem repeat and human leukocyte antigen mutations or losses confound engraftment and typing analysis in hematopoietic stem cell transplantsShalini Pereira, Tamara Vayntrub, Debra D Hiraki, et al.
The Journal of Molecular Diagnostics : JMD|July 29, 2005
Low-grade B-Cell lymphomas with plasmacytic differentiation lack PAX5 gene rearrangementsTracy I George, Joanna E Wrede, Charles D Bangs, et al.
American Journal of Clinical Pathology|September 19, 2013
Hidden mastocytosis in acute myeloid leukemia with t(8;21)(q22;q22)Ryan C Johnson, Natasha M Savage, Tsoyu Chiang, et al.
Acta Neuropathologica|July 21, 2007
Gliosarcoma with melanocytic differentiationMohanpal S Dulai, Gregory S Moes, Anita L Briley, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 26, 2013
ACMG Policy Statement. Risk categorization for oversight of laboratory-developed tests for inherited conditionsKristin G Monaghan, Judith Benkendorf, Athena M Cherry, et al.
Pediatrics|August 3, 2004
Terminal 22q deletion syndrome: a newly recognized cause of speech and language disability in the autism spectrumMelanie A Manning, Suzanne B Cassidy, Carol Clericuzio, et al.
Pageof 6