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A F Markham

Showing results (211-220 of 231) with videos related to

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Journal of Medical Genetics|September 9, 2000
A novel mutation in the mitochondrial tRNA(Ser(UCN)) gene in a family with non-syndromic sensorineural hearing impairmentT P Hutchin, M J Parker, I D Young, et al.
Human Molecular Genetics|January 1, 1996
Linkage studies of non-syndromic recessive deafness (NSRD) in a family originating from the Mirpur region of Pakistan maps DFNB1 centromeric to D13S175K A Brown, A H Janjua, G Karbani, et al.
European Journal of Human Genetics : EJHG|February 15, 2001
A new locus for autosomal recessive non-syndromal sensorineural hearing impairment (DFNB27) on chromosome 2q23-q31L J Pulleyn, A P Jackson, E Roberts, et al.
Nucleic Acids Symposium Series|January 1, 1979
Synthesis of the nascent strand of tRNAfMet from E coliE Ohtsuka, T Tanaka, S Tanaka, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 1, 1981
Total synthesis of a RNA molecule with sequence identical to that of Escherichia coli formylmethionine tRNAE Ohtsuka, S Tanaka, T Tanaka, et al.
Arthritis and Rheumatism|October 19, 2000
Fcgamma receptor type IIIA is associated with rheumatoid arthritis in two distinct ethnic groupsA W Morgan, B Griffiths, F Ponchel, et al.
European Journal of Human Genetics : EJHG|November 26, 1999
The second locus for autosomal recessive primary microcephaly (MCPH2) maps to chromosome 19q13.1-13.2E Roberts, A P Jackson, A C Carradice, et al.
The American Journal of Pathology|February 10, 2000
Localization of cyclooxygenase-2 in human sporadic colorectal adenomasK S Chapple, E J Cartwright, G Hawcroft, et al.
Journal of Medical Genetics|March 21, 1998
A Moroccan family with autosomal recessive sensorineural hearing loss caused by a mutation in the gap junction protein gene connexin 26 (GJB2)N J Lench, A F Markham, R F Mueller, et al.
Carcinogenesis|October 13, 2005
Regulation of stromal cell cyclooxygenase-2 in the ApcMin/+ mouse model of intestinal tumorigenesisM A Hull, O O Faluyi, C W S Ko, et al.
Pageof 24

Showing results (211-220 of 231) with videos related to

Sort By:
Pageof 24
Journal of Medical Genetics|September 9, 2000
A novel mutation in the mitochondrial tRNA(Ser(UCN)) gene in a family with non-syndromic sensorineural hearing impairmentT P Hutchin, M J Parker, I D Young, et al.
Human Molecular Genetics|January 1, 1996
Linkage studies of non-syndromic recessive deafness (NSRD) in a family originating from the Mirpur region of Pakistan maps DFNB1 centromeric to D13S175K A Brown, A H Janjua, G Karbani, et al.
European Journal of Human Genetics : EJHG|February 15, 2001
A new locus for autosomal recessive non-syndromal sensorineural hearing impairment (DFNB27) on chromosome 2q23-q31L J Pulleyn, A P Jackson, E Roberts, et al.
Nucleic Acids Symposium Series|January 1, 1979
Synthesis of the nascent strand of tRNAfMet from E coliE Ohtsuka, T Tanaka, S Tanaka, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 1, 1981
Total synthesis of a RNA molecule with sequence identical to that of Escherichia coli formylmethionine tRNAE Ohtsuka, S Tanaka, T Tanaka, et al.
Arthritis and Rheumatism|October 19, 2000
Fcgamma receptor type IIIA is associated with rheumatoid arthritis in two distinct ethnic groupsA W Morgan, B Griffiths, F Ponchel, et al.
European Journal of Human Genetics : EJHG|November 26, 1999
The second locus for autosomal recessive primary microcephaly (MCPH2) maps to chromosome 19q13.1-13.2E Roberts, A P Jackson, A C Carradice, et al.
The American Journal of Pathology|February 10, 2000
Localization of cyclooxygenase-2 in human sporadic colorectal adenomasK S Chapple, E J Cartwright, G Hawcroft, et al.
Journal of Medical Genetics|March 21, 1998
A Moroccan family with autosomal recessive sensorineural hearing loss caused by a mutation in the gap junction protein gene connexin 26 (GJB2)N J Lench, A F Markham, R F Mueller, et al.
Carcinogenesis|October 13, 2005
Regulation of stromal cell cyclooxygenase-2 in the ApcMin/+ mouse model of intestinal tumorigenesisM A Hull, O O Faluyi, C W S Ko, et al.
Pageof 24