Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

O M Garson

Showing results (21-30 of 103) with videos related to

Pageof 11
Sort By:
Leukemia|January 1, 1994
The prognostic significance of deletion of the long arm of chromosome 20 in myeloid disordersL J Campbell, O M Garson
Haematologia|January 1, 1974
Chromosome changes in the blastic transformation stage of chronic granulocytic leukaemiaO M Garson, G C de Gruchy
Cancer Genetics and Cytogenetics|March 1, 1984
Fourth International Workshop on Chromosomes in Leukemia 1982: Translocation (8;21)(q22;q22) in acute nonlymphocytic leukemiaA Hagemeijer, O M Garson, K Kondo
Cancer Genetics and Cytogenetics|September 1, 1982
Double 9;22 translocation with hyperdiploidy appearing in blastic transformation of chronic granulocytic leukemiaP Rajasekariah, I Illes, O M Garson
Australian and New Zealand Journal of Medicine|June 1, 1978
A variant chromosomal translocation found in a series of 24 patients with Philadelphia positive chronic granulocytic leukaemiaJ M Lyall, G N Brodie, O M Garson
Medical and Pediatric Oncology|January 1, 1990
Acute nonlymphocytic leukemia after transient myeloproliferative disorder in a patient with Down syndromeP L Barnett, A C Clark, O M Garson
Genes, Chromosomes & Cancer|August 1, 1993
Co-amplification of the gene for parathyroid hormone-related protein (PTHRP) and KRAS2 in a human lung cancer cell lineC Rudduck, L Duncan, R Center, et al.
British Journal of Haematology|June 1, 1972
Clinical and cytogenetic studies in chronic myelomonocytic leukaemiaA D Hurdle, O M Garson, D G Buist
Cancer Genetics and Cytogenetics|August 1, 1984
Translocation 1;19--a new cytogenetic abnormality in acute lymphocytic leukemiaP M Michael, M D Levin, O M Garson
The Medical Journal of Australia|August 1, 1970
Coexisting familial abnormalities of karyotype and phenotype. Chromosome 16 and an unusual form of cutis laxa with skin websO M Garson, A G Baikie, B M O'Brien
Pageof 11

Showing results (21-30 of 103) with videos related to

Sort By:
Pageof 11
Leukemia|January 1, 1994
The prognostic significance of deletion of the long arm of chromosome 20 in myeloid disordersL J Campbell, O M Garson
Haematologia|January 1, 1974
Chromosome changes in the blastic transformation stage of chronic granulocytic leukaemiaO M Garson, G C de Gruchy
Cancer Genetics and Cytogenetics|March 1, 1984
Fourth International Workshop on Chromosomes in Leukemia 1982: Translocation (8;21)(q22;q22) in acute nonlymphocytic leukemiaA Hagemeijer, O M Garson, K Kondo
Cancer Genetics and Cytogenetics|September 1, 1982
Double 9;22 translocation with hyperdiploidy appearing in blastic transformation of chronic granulocytic leukemiaP Rajasekariah, I Illes, O M Garson
Australian and New Zealand Journal of Medicine|June 1, 1978
A variant chromosomal translocation found in a series of 24 patients with Philadelphia positive chronic granulocytic leukaemiaJ M Lyall, G N Brodie, O M Garson
Medical and Pediatric Oncology|January 1, 1990
Acute nonlymphocytic leukemia after transient myeloproliferative disorder in a patient with Down syndromeP L Barnett, A C Clark, O M Garson
Genes, Chromosomes & Cancer|August 1, 1993
Co-amplification of the gene for parathyroid hormone-related protein (PTHRP) and KRAS2 in a human lung cancer cell lineC Rudduck, L Duncan, R Center, et al.
British Journal of Haematology|June 1, 1972
Clinical and cytogenetic studies in chronic myelomonocytic leukaemiaA D Hurdle, O M Garson, D G Buist
Cancer Genetics and Cytogenetics|August 1, 1984
Translocation 1;19--a new cytogenetic abnormality in acute lymphocytic leukemiaP M Michael, M D Levin, O M Garson
The Medical Journal of Australia|August 1, 1970
Coexisting familial abnormalities of karyotype and phenotype. Chromosome 16 and an unusual form of cutis laxa with skin websO M Garson, A G Baikie, B M O'Brien
Pageof 11