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J Buckle

Showing results (51-60 of 137) with videos related to

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Nucleic Acids Research|September 11, 1992
Structure of the human DNA repair gene HAP1 and its localisation to chromosome 14q 11.2-12C N Robson, D Hochhauser, R Craig, et al.
Human Molecular Genetics|August 1, 1994
Dissecting the centromere of the human Y chromosome with cloned telomeric DNAK E Brown, M A Barnett, C Burgtorf, et al.
Cancer Genetics and Cytogenetics|May 1, 1991
Translocation 1;7 in hematologic disorders--a report of three further cases. Absence of amplification of the gene for the epidermal growth factor receptorG M Abrahamson, K Rack, V J Buckle, et al.
Cell|October 5, 1990
Structure and polymorphism of human telomere-associated DNAW R Brown, P J MacKinnon, A Villasanté, et al.
American Journal of Hematology|February 1, 1993
Comparison of cytogenetic and restriction fragment length polymorphism analyses for the detection of loss of chromosome material in clonal hemopoietic disordersG M Abrahamson, K Rack, D G Oscier, et al.
Blood|August 1, 1984
A new translocation, t(1;3) (p36;q21), in myelodysplastic disordersD J Moir, P A Jones, J Pearson, et al.
Human Molecular Genetics|March 28, 2015
Expanded GAA repeats impair FXN gene expression and reposition the FXN locus to the nuclear lamina in single cellsAna M Silva, Jill M Brown, Veronica J Buckle, 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 chromosomeY Boyd, V J Buckle, E A Munro, et al.
Nature Genetics|February 1, 1995
The detection of subtelomeric chromosomal rearrangements in idiopathic mental retardationJ Flint, A O Wilkie, V J Buckle, et al.
Genomics|September 1, 1987
Chromosome maps of man and mouse, IIIA G Searle, J Peters, M F Lyon, et al.
Pageof 14

Showing results (51-60 of 137) with videos related to

Sort By:
Pageof 14
Nucleic Acids Research|September 11, 1992
Structure of the human DNA repair gene HAP1 and its localisation to chromosome 14q 11.2-12C N Robson, D Hochhauser, R Craig, et al.
Human Molecular Genetics|August 1, 1994
Dissecting the centromere of the human Y chromosome with cloned telomeric DNAK E Brown, M A Barnett, C Burgtorf, et al.
Cancer Genetics and Cytogenetics|May 1, 1991
Translocation 1;7 in hematologic disorders--a report of three further cases. Absence of amplification of the gene for the epidermal growth factor receptorG M Abrahamson, K Rack, V J Buckle, et al.
Cell|October 5, 1990
Structure and polymorphism of human telomere-associated DNAW R Brown, P J MacKinnon, A Villasanté, et al.
American Journal of Hematology|February 1, 1993
Comparison of cytogenetic and restriction fragment length polymorphism analyses for the detection of loss of chromosome material in clonal hemopoietic disordersG M Abrahamson, K Rack, D G Oscier, et al.
Blood|August 1, 1984
A new translocation, t(1;3) (p36;q21), in myelodysplastic disordersD J Moir, P A Jones, J Pearson, et al.
Human Molecular Genetics|March 28, 2015
Expanded GAA repeats impair FXN gene expression and reposition the FXN locus to the nuclear lamina in single cellsAna M Silva, Jill M Brown, Veronica J Buckle, 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 chromosomeY Boyd, V J Buckle, E A Munro, et al.
Nature Genetics|February 1, 1995
The detection of subtelomeric chromosomal rearrangements in idiopathic mental retardationJ Flint, A O Wilkie, V J Buckle, et al.
Genomics|September 1, 1987
Chromosome maps of man and mouse, IIIA G Searle, J Peters, M F Lyon, et al.
Pageof 14