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American Journal of Medical Genetics
|
June 1, 1993
Confirmation of trisomy 22 in two cases using chromosome painting: comparison with t(11;22)
H R Slater, L E Voullaire, C E Vaux, et al.
Nature
|
May 12, 1983
Gene deletions in patients with haemophilia B and anti-factor IX antibodies
F Giannelli, K H Choo, D J Rees, et al.
The Journal of Biological Chemistry
|
March 10, 1995
Enhanced sensitivity to oxidative stress in cultured embryonic cells from transgenic mice deficient in metallothionein I and II genes
J S Lazo, Y Kondo, D Dellapiazza, et al.
Journal of Medical Genetics
|
December 14, 1999
Neocentromere formation in a stable ring 1p32-p36.1 chromosome
H R Slater, S Nouri, E Earle, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
March 24, 1999
Cloning, expression, and promoter structure of a mammalian inner centromere protein (INCENP)
R Saffery, D V Irvine, B T Kile, et al.
Annals of Human Genetics
|
May 1, 1984
Assignment of the haemophilia B (factor IX) locus to the q26-qter region of the X chromosome
Y Boyd, V J Buckle, E A Munro, et al.
Lancet (London, England)
|
August 11, 1984
Linkage analysis of X-linked mental retardation with and without fragile-X using factor IX gene probe
K H Choo, D George, G Filby, et al.
Genome Research
|
March 7, 2001
A novel chromatin immunoprecipitation and array (CIA) analysis identifies a 460-kb CENP-A-binding neocentromere DNA
A W Lo, D J Magliano, M C Sibson, et al.
American Journal of Medical Genetics
|
July 15, 1994
Regional localisation of a non-specific X-linked mental retardation gene (MRX19) to Xp22
A J Donnelly, K H Choo, H M Kozman, et al.
International Immunology
|
September 1, 1992
The gene organization of the human beta 7 subunit, the common beta subunit of the leukocyte integrins HML-1 and LPAM-1
W M Jiang, D Jenkins, Q Yuan, et al.
Page
of 12
Search research articles
Search
Showing results (81-90 of 117) with videos related to
Sort By:
Page
of 12
American Journal of Medical Genetics
|
June 1, 1993
Confirmation of trisomy 22 in two cases using chromosome painting: comparison with t(11;22)
H R Slater, L E Voullaire, C E Vaux, et al.
Nature
|
May 12, 1983
Gene deletions in patients with haemophilia B and anti-factor IX antibodies
F Giannelli, K H Choo, D J Rees, et al.
The Journal of Biological Chemistry
|
March 10, 1995
Enhanced sensitivity to oxidative stress in cultured embryonic cells from transgenic mice deficient in metallothionein I and II genes
J S Lazo, Y Kondo, D Dellapiazza, et al.
Journal of Medical Genetics
|
December 14, 1999
Neocentromere formation in a stable ring 1p32-p36.1 chromosome
H R Slater, S Nouri, E Earle, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
March 24, 1999
Cloning, expression, and promoter structure of a mammalian inner centromere protein (INCENP)
R Saffery, D V Irvine, B T Kile, et al.
Annals of Human Genetics
|
May 1, 1984
Assignment of the haemophilia B (factor IX) locus to the q26-qter region of the X chromosome
Y Boyd, V J Buckle, E A Munro, et al.
Lancet (London, England)
|
August 11, 1984
Linkage analysis of X-linked mental retardation with and without fragile-X using factor IX gene probe
K H Choo, D George, G Filby, et al.
Genome Research
|
March 7, 2001
A novel chromatin immunoprecipitation and array (CIA) analysis identifies a 460-kb CENP-A-binding neocentromere DNA
A W Lo, D J Magliano, M C Sibson, et al.
American Journal of Medical Genetics
|
July 15, 1994
Regional localisation of a non-specific X-linked mental retardation gene (MRX19) to Xp22
A J Donnelly, K H Choo, H M Kozman, et al.
International Immunology
|
September 1, 1992
The gene organization of the human beta 7 subunit, the common beta subunit of the leukocyte integrins HML-1 and LPAM-1
W M Jiang, D Jenkins, Q Yuan, et al.
Page
of 12