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H F Mark

Showing results (31-40 of 104) with videos related to

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Pathobiology : Journal of Immunopathology, Molecular and Cellular Biology|January 5, 1999
Conventional and molecular cytogenetic identification of a variant klinefelter syndrome patient with a deleted X chromosomeH F Mark, D Feldman, M Sigman
Archives of Pathology & Laboratory Medicine|March 23, 1999
Klinefelter syndromeH F Mark, D Alter, P Mousseau
Cancer Genetics and Cytogenetics|February 12, 1999
Trisomy 10 as a sole chromosomal abnormality in AML-M2O Estalilla, P Rintels, H F Mark
Cancer Genetics and Cytogenetics|February 14, 1998
Trisomy 10 in leukemiaO Estalilla, P Rintels, H F Mark
Experimental and Molecular Pathology|September 16, 1999
Occurrence of both t(1;19) and t(8;14) in a patient with chronic lymphocytic leukemiaH F Mark, E Sotomayor, A Mega
Medicine and Health, Rhode Island|June 9, 1998
Advances in breast cancer geneticsH F Mark, M McCarthy, D Berry
Cancer Genetics and Cytogenetics|December 22, 1999
Discordant detection of monosomy 7 by GTG-banding and FISH in a patient with Shwachman-Diamond syndrome without evidence of myelodysplastic syndrome or acute myelogenous leukemiaR A Sokolic, W Ferguson, H F Mark
Clinical Pediatrics|April 1, 1995
Developmental delay caused by a supernumerary chromosome, inv dup (15), identified by fluorescent in situ hybridizationD Abuelo, H F Mark, J A Bier
Annals of Clinical and Laboratory Science|July 1, 1996
The frequency of chromosomal abnormalities in patients referred for fragile X analysisH F Mark, J A Bier, P Scola
Breast Cancer Research and Treatment|January 1, 1996
Fluorescent in situ hybridization assessment of chromosome 8 copy number in breast cancerA Afify, K I Bland, H F Mark
Pageof 11

Showing results (31-40 of 104) with videos related to

Sort By:
Pageof 11
Pathobiology : Journal of Immunopathology, Molecular and Cellular Biology|January 5, 1999
Conventional and molecular cytogenetic identification of a variant klinefelter syndrome patient with a deleted X chromosomeH F Mark, D Feldman, M Sigman
Archives of Pathology & Laboratory Medicine|March 23, 1999
Klinefelter syndromeH F Mark, D Alter, P Mousseau
Cancer Genetics and Cytogenetics|February 12, 1999
Trisomy 10 as a sole chromosomal abnormality in AML-M2O Estalilla, P Rintels, H F Mark
Cancer Genetics and Cytogenetics|February 14, 1998
Trisomy 10 in leukemiaO Estalilla, P Rintels, H F Mark
Experimental and Molecular Pathology|September 16, 1999
Occurrence of both t(1;19) and t(8;14) in a patient with chronic lymphocytic leukemiaH F Mark, E Sotomayor, A Mega
Medicine and Health, Rhode Island|June 9, 1998
Advances in breast cancer geneticsH F Mark, M McCarthy, D Berry
Cancer Genetics and Cytogenetics|December 22, 1999
Discordant detection of monosomy 7 by GTG-banding and FISH in a patient with Shwachman-Diamond syndrome without evidence of myelodysplastic syndrome or acute myelogenous leukemiaR A Sokolic, W Ferguson, H F Mark
Clinical Pediatrics|April 1, 1995
Developmental delay caused by a supernumerary chromosome, inv dup (15), identified by fluorescent in situ hybridizationD Abuelo, H F Mark, J A Bier
Annals of Clinical and Laboratory Science|July 1, 1996
The frequency of chromosomal abnormalities in patients referred for fragile X analysisH F Mark, J A Bier, P Scola
Breast Cancer Research and Treatment|January 1, 1996
Fluorescent in situ hybridization assessment of chromosome 8 copy number in breast cancerA Afify, K I Bland, H F Mark
Pageof 11