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Nature Genetics
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February 1, 1995
The detection of subtelomeric chromosomal rearrangements in idiopathic mental retardation
J Flint, A O Wilkie, V J Buckle, et al.
Genomics
|
September 1, 1987
Chromosome maps of man and mouse, III
A G Searle, J Peters, M F Lyon, et al.
British Journal of Haematology
|
October 1, 1990
Homozygous deletion of FMS in a patient with the 5q- syndrome
J Boultwood, K Rack, V J Buckle, et al.
International Journal of Radiation Biology
|
March 1, 1995
Radiation-induced genomic instability: delayed cytogenetic aberrations and apoptosis in primary human bone marrow cells
M A Kadhim, S A Lorimore, K M Townsend, et al.
Genomics
|
August 1, 1989
Localization of human monoamine oxidase-A gene to Xp11.23-11.4 by in situ hybridization: implications for Norrie disease
E R Levy, J F Powell, V J Buckle, et al.
Journal of Medical Genetics
|
April 1, 1987
Localisation of Y chromosome sequences in normal and 'XX' males
V J Buckle, Y Boyd, N Fraser, et al.
Nature Genetics
|
December 1, 1992
Targeted breakage of a human chromosome mediated by cloned human telomeric DNA
J E Itzhaki, M A Barnett, A B MacCarthy, et al.
Lancet (London, England)
|
October 8, 1994
Alpha-particle-induced chromosomal instability in human bone marrow cells
M A Kadhim, S A Lorimore, M D Hepburn, et al.
British Journal of Haematology
|
December 1, 1991
Clonality of cell populations in refractory anaemia using combined approach of gene loss and X-linked restriction fragment length polymorphism-methylation analyses
G Abrahamson, J Boultwood, J Madden, et al.
Human Molecular Genetics
|
February 1, 1993
The identification of a third fragile site, FRAXF, in Xq27--q28 distal to both FRAXA and FRAXE
M C Hirst, A Barnicoat, G Flynn, et al.
Page
of 6
Search research articles
Search
Showing results (21-30 of 56) with videos related to
Sort By:
Page
of 6
Nature Genetics
|
February 1, 1995
The detection of subtelomeric chromosomal rearrangements in idiopathic mental retardation
J Flint, A O Wilkie, V J Buckle, et al.
Genomics
|
September 1, 1987
Chromosome maps of man and mouse, III
A G Searle, J Peters, M F Lyon, et al.
British Journal of Haematology
|
October 1, 1990
Homozygous deletion of FMS in a patient with the 5q- syndrome
J Boultwood, K Rack, V J Buckle, et al.
International Journal of Radiation Biology
|
March 1, 1995
Radiation-induced genomic instability: delayed cytogenetic aberrations and apoptosis in primary human bone marrow cells
M A Kadhim, S A Lorimore, K M Townsend, et al.
Genomics
|
August 1, 1989
Localization of human monoamine oxidase-A gene to Xp11.23-11.4 by in situ hybridization: implications for Norrie disease
E R Levy, J F Powell, V J Buckle, et al.
Journal of Medical Genetics
|
April 1, 1987
Localisation of Y chromosome sequences in normal and 'XX' males
V J Buckle, Y Boyd, N Fraser, et al.
Nature Genetics
|
December 1, 1992
Targeted breakage of a human chromosome mediated by cloned human telomeric DNA
J E Itzhaki, M A Barnett, A B MacCarthy, et al.
Lancet (London, England)
|
October 8, 1994
Alpha-particle-induced chromosomal instability in human bone marrow cells
M A Kadhim, S A Lorimore, M D Hepburn, et al.
British Journal of Haematology
|
December 1, 1991
Clonality of cell populations in refractory anaemia using combined approach of gene loss and X-linked restriction fragment length polymorphism-methylation analyses
G Abrahamson, J Boultwood, J Madden, et al.
Human Molecular Genetics
|
February 1, 1993
The identification of a third fragile site, FRAXF, in Xq27--q28 distal to both FRAXA and FRAXE
M C Hirst, A Barnicoat, G Flynn, et al.
Page
of 6