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J D Brook

Showing results (21-30 of 72) with videos related to

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Human Genetics|August 1, 1989
Long-range restriction map of a region of human chromosome 19 containing the apolipoprotein genes, a CLL-associated translocation breakpoint, and two polymorphic MluI sitesD J Shaw, H G Harley, J D Brook, et al.
Journal of Medical Genetics|December 19, 2001
Detection of a large TBX5 deletion in a family with Holt-Oram syndromeS M Akrami, R M Winter, J D Brook, et al.
Somatic Cell and Molecular Genetics|July 1, 1986
Mapping human chromosomes in somatic cell hybrids using a low-copy-number repetitive sequenceD J Shaw, J D Brook, C S Brown, et al.
Journal of Medical Genetics|February 9, 1999
Myotonic dystrophy: the correlation of (CTG) repeat length in leucocytes with age at onset is significant only for patients with small expansionsM G Hamshere, H Harley, P Harper, et al.
Cancer Research|December 1, 1996
High levels of allele loss at the FHIT and ATM genes in non-comedo ductal carcinoma in situ and grade I tubular invasive breast cancersS Man, I O Ellis, M Sibbering, et al.
Somatic Cell and Molecular Genetics|November 1, 1986
Chromosomal assignment of c-MEL, a human transforming oncogene, to chromosome 19 (p13.2-q13.2)N K Spurr, D Hughes, P N Goodfellow, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 8, 1997
Transcriptional abnormality in myotonic dystrophy affects DMPK but not neighboring genesM G Hamshere, E E Newman, M Alwazzan, et al.
Human Genetics|January 1, 1984
Localisation of genetic markers and orientation of the linkage group on chromosome 19J D Brook, D J Shaw, L Meredith, et al.
Nucleic Acids Research|February 25, 1990
RFLP for a DNA clone which maps to 19q13.2-19qter (D19S63)J D Brook, H G Harley, S A Rundle, et al.
Human Molecular Genetics|September 1, 1992
Insertion/deletion polymorphism at D19S95 associated with the myotonic dystrophy CTG repeatS R Crow, H G Harley, J D Brook, et al.
Pageof 8

Showing results (21-30 of 72) with videos related to

Sort By:
Pageof 8
Human Genetics|August 1, 1989
Long-range restriction map of a region of human chromosome 19 containing the apolipoprotein genes, a CLL-associated translocation breakpoint, and two polymorphic MluI sitesD J Shaw, H G Harley, J D Brook, et al.
Journal of Medical Genetics|December 19, 2001
Detection of a large TBX5 deletion in a family with Holt-Oram syndromeS M Akrami, R M Winter, J D Brook, et al.
Somatic Cell and Molecular Genetics|July 1, 1986
Mapping human chromosomes in somatic cell hybrids using a low-copy-number repetitive sequenceD J Shaw, J D Brook, C S Brown, et al.
Journal of Medical Genetics|February 9, 1999
Myotonic dystrophy: the correlation of (CTG) repeat length in leucocytes with age at onset is significant only for patients with small expansionsM G Hamshere, H Harley, P Harper, et al.
Cancer Research|December 1, 1996
High levels of allele loss at the FHIT and ATM genes in non-comedo ductal carcinoma in situ and grade I tubular invasive breast cancersS Man, I O Ellis, M Sibbering, et al.
Somatic Cell and Molecular Genetics|November 1, 1986
Chromosomal assignment of c-MEL, a human transforming oncogene, to chromosome 19 (p13.2-q13.2)N K Spurr, D Hughes, P N Goodfellow, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 8, 1997
Transcriptional abnormality in myotonic dystrophy affects DMPK but not neighboring genesM G Hamshere, E E Newman, M Alwazzan, et al.
Human Genetics|January 1, 1984
Localisation of genetic markers and orientation of the linkage group on chromosome 19J D Brook, D J Shaw, L Meredith, et al.
Nucleic Acids Research|February 25, 1990
RFLP for a DNA clone which maps to 19q13.2-19qter (D19S63)J D Brook, H G Harley, S A Rundle, et al.
Human Molecular Genetics|September 1, 1992
Insertion/deletion polymorphism at D19S95 associated with the myotonic dystrophy CTG repeatS R Crow, H G Harley, J D Brook, et al.
Pageof 8