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Nederlands Tijdschrift Voor Geneeskunde
|
May 2, 1992
[Molecular genetic studies in alpha-thalassemia]
D de Korte, H T Cuypers, A de Klein, et al.
The Journal of Steroid Biochemistry and Molecular Biology
|
December 20, 1990
Genetic changes in somatostatin receptor positive breast tumors
A H Bootsma, A de Klein, J C Reubi, et al.
British Journal of Cancer
|
June 20, 2013
Patient survival in uveal melanoma is not affected by oncogenic mutations in GNAQ and GNA11
A E Koopmans, J Vaarwater, D Paridaens, et al.
Cell
|
January 1, 1984
Philadelphia chromosomal breakpoints are clustered within a limited region, bcr, on chromosome 22
J Groffen, J R Stephenson, N Heisterkamp, et al.
American Journal of Human Genetics
|
April 17, 2007
Genetic factors in congenital diaphragmatic hernia
A M Holder, M Klaassens, D Tibboel, et al.
Molecular and Cellular Biology
|
February 1, 1985
Translocation of oncogene c-sis from chromosome 22 to chromosome 11 in a Ewing sarcoma-derived cell line
A G van Kessel, C Turc-Carel, A de Klein, et al.
Leukemia
|
January 22, 1998
Development of an interphase fluorescent in situ hybridization (FISH) test to detect t(8;21) in AML patients
A Hagemeijer, A de Klein, J Wijsman, et al.
Haematologica
|
November 1, 1987
The c-abl oncogene in chronic myelogenous leukemia
A de Klein, C R Bartram, A Hagemeijer, et al.
The EMBO Journal
|
March 1, 1985
C-abl and bcr are rearranged in a Ph1-negative CML patient
C R Bartram, E Kleihauer, A de Klein, et al.
Clinical Genetics
|
April 22, 2004
Deletion of the TWIST gene in a large five-generation family
I M De Heer, A J M Hoogeboom, H J Eussen, et al.
Page
of 9
Search research articles
Search
Showing results (21-30 of 83) with videos related to
Sort By:
Page
of 9
Nederlands Tijdschrift Voor Geneeskunde
|
May 2, 1992
[Molecular genetic studies in alpha-thalassemia]
D de Korte, H T Cuypers, A de Klein, et al.
The Journal of Steroid Biochemistry and Molecular Biology
|
December 20, 1990
Genetic changes in somatostatin receptor positive breast tumors
A H Bootsma, A de Klein, J C Reubi, et al.
British Journal of Cancer
|
June 20, 2013
Patient survival in uveal melanoma is not affected by oncogenic mutations in GNAQ and GNA11
A E Koopmans, J Vaarwater, D Paridaens, et al.
Cell
|
January 1, 1984
Philadelphia chromosomal breakpoints are clustered within a limited region, bcr, on chromosome 22
J Groffen, J R Stephenson, N Heisterkamp, et al.
American Journal of Human Genetics
|
April 17, 2007
Genetic factors in congenital diaphragmatic hernia
A M Holder, M Klaassens, D Tibboel, et al.
Molecular and Cellular Biology
|
February 1, 1985
Translocation of oncogene c-sis from chromosome 22 to chromosome 11 in a Ewing sarcoma-derived cell line
A G van Kessel, C Turc-Carel, A de Klein, et al.
Leukemia
|
January 22, 1998
Development of an interphase fluorescent in situ hybridization (FISH) test to detect t(8;21) in AML patients
A Hagemeijer, A de Klein, J Wijsman, et al.
Haematologica
|
November 1, 1987
The c-abl oncogene in chronic myelogenous leukemia
A de Klein, C R Bartram, A Hagemeijer, et al.
The EMBO Journal
|
March 1, 1985
C-abl and bcr are rearranged in a Ph1-negative CML patient
C R Bartram, E Kleihauer, A de Klein, et al.
Clinical Genetics
|
April 22, 2004
Deletion of the TWIST gene in a large five-generation family
I M De Heer, A J M Hoogeboom, H J Eussen, et al.
Page
of 9