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Journal of Pediatric Hematology/Oncology
|
February 25, 1999
Multifocal osteosarcoma: an unusual presentation
S Gunawardena, M Chintagumpala, L Trautwein, et al.
The Journal of Molecular Diagnostics : JMD
|
March 27, 2007
Guidance for fluorescence in situ hybridization testing in hematologic disorders
Daynna J Wolff, Adam Bagg, Linda D Cooley, et al.
Ultrastructural Pathology
|
September 1, 1995
Malignant melanoma of soft parts involving the head and neck region: review of literature and case report
M J Hicks, V A Saldivar, M M Chintagumpala, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 30, 2019
Technical laboratory standards for interpretation and reporting of acquired copy-number abnormalities and copy-neutral loss of heterozygosity in neoplastic disorders: a joint consensus recommendation from the American College of Medical Genetics and Genomics (ACMG) and the Cancer Genomics Consortium (CGC)
Fady M Mikhail, Jaclyn A Biegel, Linda D Cooley, et al.
Journal of Clinical Microbiology
|
July 16, 1999
Performance of the Affymetrix GeneChip HIV PRT 440 platform for antiretroviral drug resistance genotyping of human immunodeficiency virus type 1 clades and viral isolates with length polymorphisms
M Vahey, M E Nau, S Barrick, et al.
European Journal of Medical Genetics
|
March 6, 2019
CNTN6 copy number variations: Uncertain clinical significance in individuals with neurodevelopmental disorders
Elena A Repnikova, Dmitry A Lyalin, Kimberly McDonald, et al.
Cancer Genetics and Cytogenetics
|
June 9, 2007
Prognostic significance of cytogenetically detected chromosome 21 anomalies in childhood acute lymphoblastic leukemia: a Pediatric Oncology Group study
Linda D Cooley, Saleen Chenevert, Jonathan J Shuster, et al.
Journal of Neuroinflammation
|
December 15, 2017
Human microglia and astrocytes constitutively express the neurokinin-1 receptor and functionally respond to substance P
Amanda R Burmeister, M Brittany Johnson, Vinita S Chauhan, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
September 23, 2003
Problems with ISCN FISH Nomenclature make it not practical for use in clinical test reports or cytogenetic databases [corrected]
James T Mascarello, Linda D Cooley, Keri Davison, et al.
Leukemia
|
February 18, 2005
Accumulation of methotrexate and methotrexate polyglutamates in lymphoblasts and treatment outcome in children with B-progenitor-cell acute lymphoblastic leukemia: a Pediatric Oncology Group study
V M Whitehead, J J Shuster, M J Vuchich, et al.
Page
of 13
Search research articles
Search
Showing results (91-100 of 121) with videos related to
Sort By:
Page
of 13
Journal of Pediatric Hematology/Oncology
|
February 25, 1999
Multifocal osteosarcoma: an unusual presentation
S Gunawardena, M Chintagumpala, L Trautwein, et al.
The Journal of Molecular Diagnostics : JMD
|
March 27, 2007
Guidance for fluorescence in situ hybridization testing in hematologic disorders
Daynna J Wolff, Adam Bagg, Linda D Cooley, et al.
Ultrastructural Pathology
|
September 1, 1995
Malignant melanoma of soft parts involving the head and neck region: review of literature and case report
M J Hicks, V A Saldivar, M M Chintagumpala, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 30, 2019
Technical laboratory standards for interpretation and reporting of acquired copy-number abnormalities and copy-neutral loss of heterozygosity in neoplastic disorders: a joint consensus recommendation from the American College of Medical Genetics and Genomics (ACMG) and the Cancer Genomics Consortium (CGC)
Fady M Mikhail, Jaclyn A Biegel, Linda D Cooley, et al.
Journal of Clinical Microbiology
|
July 16, 1999
Performance of the Affymetrix GeneChip HIV PRT 440 platform for antiretroviral drug resistance genotyping of human immunodeficiency virus type 1 clades and viral isolates with length polymorphisms
M Vahey, M E Nau, S Barrick, et al.
European Journal of Medical Genetics
|
March 6, 2019
CNTN6 copy number variations: Uncertain clinical significance in individuals with neurodevelopmental disorders
Elena A Repnikova, Dmitry A Lyalin, Kimberly McDonald, et al.
Cancer Genetics and Cytogenetics
|
June 9, 2007
Prognostic significance of cytogenetically detected chromosome 21 anomalies in childhood acute lymphoblastic leukemia: a Pediatric Oncology Group study
Linda D Cooley, Saleen Chenevert, Jonathan J Shuster, et al.
Journal of Neuroinflammation
|
December 15, 2017
Human microglia and astrocytes constitutively express the neurokinin-1 receptor and functionally respond to substance P
Amanda R Burmeister, M Brittany Johnson, Vinita S Chauhan, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
September 23, 2003
Problems with ISCN FISH Nomenclature make it not practical for use in clinical test reports or cytogenetic databases [corrected]
James T Mascarello, Linda D Cooley, Keri Davison, et al.
Leukemia
|
February 18, 2005
Accumulation of methotrexate and methotrexate polyglutamates in lymphoblasts and treatment outcome in children with B-progenitor-cell acute lymphoblastic leukemia: a Pediatric Oncology Group study
V M Whitehead, J J Shuster, M J Vuchich, et al.
Page
of 13