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Genes, Chromosomes & Cancer
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July 1, 1994
Characterization of homogeneously staining regions in a small cell lung cancer cell line, using in situ hybridization with an MYCN probe
E Dietzsch, R E Lukeis, V Vrazas, et al.
Journal of Mental Deficiency Research
|
March 1, 1974
A girl with Wolf-Hirschorn syndrome and mosaicism 46,XX-46,XX,4p-
C G Judge, O M Garson, D B Pitt, et al.
Cancer Genetics and Cytogenetics
|
January 1, 1988
Isodicentric X chromosomes involving the Xq13 breakpoint in myelodysplasia and acute nonlymphocytic leukemia
W B Mackinnon, P M Michael, L M Webber, et al.
Australian Paediatric Journal
|
March 1, 1970
Down's Syndrome with translocation-en-tandem: a report of two unrelated cases
O M Garson, A G Baikie, D B Pitt, et al.
British Journal of Plastic Surgery
|
October 1, 1970
Multiple congenital skin webbing with cutis laxa
B M O'Brien, O M Garson, A G Baikie, et al.
Immunogenetics
|
January 1, 1993
The human FCG1 gene encoding the high-affinity Fc gamma RI maps to chromosome 1q21
E Dietzsch, N Osman, I F McKenzie, et al.
Cytogenetics and Cell Genetics
|
January 1, 1992
Regional localization of the gene for clusterin (SP-40,40; gene symbol CLI) to human chromosome 8p12-->p21
E Dietzsch, B F Murphy, L Kirszbaum, et al.
Leukemia Research
|
January 1, 1986
Elevation of c-abl-mRNA in human leukemic B lymphoblasts
T de Kretser, F Adams, L Devereux, et al.
Cancer Genetics and Cytogenetics
|
June 1, 1990
Establishment and characterization of a childhood pre-B acute lymphoblastic leukemia cell line, PER-278, with chromosome translocations t(1;19) and t(1;9)
U R Kees, R Lukeis, J Ford, et al.
Pathology
|
January 1, 1984
Clinicopathological characteristics of acute lymphoblastic leukemia with the 4;11 chromosome translocation
M D Levin, P M Michael, O M Garson, et al.
Page
of 12
Search research articles
Search
Showing results (61-70 of 115) with videos related to
Sort By:
Page
of 12
Genes, Chromosomes & Cancer
|
July 1, 1994
Characterization of homogeneously staining regions in a small cell lung cancer cell line, using in situ hybridization with an MYCN probe
E Dietzsch, R E Lukeis, V Vrazas, et al.
Journal of Mental Deficiency Research
|
March 1, 1974
A girl with Wolf-Hirschorn syndrome and mosaicism 46,XX-46,XX,4p-
C G Judge, O M Garson, D B Pitt, et al.
Cancer Genetics and Cytogenetics
|
January 1, 1988
Isodicentric X chromosomes involving the Xq13 breakpoint in myelodysplasia and acute nonlymphocytic leukemia
W B Mackinnon, P M Michael, L M Webber, et al.
Australian Paediatric Journal
|
March 1, 1970
Down's Syndrome with translocation-en-tandem: a report of two unrelated cases
O M Garson, A G Baikie, D B Pitt, et al.
British Journal of Plastic Surgery
|
October 1, 1970
Multiple congenital skin webbing with cutis laxa
B M O'Brien, O M Garson, A G Baikie, et al.
Immunogenetics
|
January 1, 1993
The human FCG1 gene encoding the high-affinity Fc gamma RI maps to chromosome 1q21
E Dietzsch, N Osman, I F McKenzie, et al.
Cytogenetics and Cell Genetics
|
January 1, 1992
Regional localization of the gene for clusterin (SP-40,40; gene symbol CLI) to human chromosome 8p12-->p21
E Dietzsch, B F Murphy, L Kirszbaum, et al.
Leukemia Research
|
January 1, 1986
Elevation of c-abl-mRNA in human leukemic B lymphoblasts
T de Kretser, F Adams, L Devereux, et al.
Cancer Genetics and Cytogenetics
|
June 1, 1990
Establishment and characterization of a childhood pre-B acute lymphoblastic leukemia cell line, PER-278, with chromosome translocations t(1;19) and t(1;9)
U R Kees, R Lukeis, J Ford, et al.
Pathology
|
January 1, 1984
Clinicopathological characteristics of acute lymphoblastic leukemia with the 4;11 chromosome translocation
M D Levin, P M Michael, O M Garson, et al.
Page
of 12