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S D Wilton

Showing results (31-40 of 52) with videos related to

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Cytogenetics and Cell Genetics|January 1, 1993
Assignment of the human slow skeletal muscle troponin gene (TNNI1) to 1q32 by fluorescence in situ hybridisationH J Eyre, P A Akkari, C Meredith, et al.
Neuromuscular Disorders : NMD|January 5, 2000
Homozygosity for a nonsense mutation in the alpha-tropomyosin slow gene TPM3 in a patient with severe infantile nemaline myopathyP Tan, J Briner, E Boltshauser, et al.
Cytogenetics and Cell Genetics|January 1, 1996
Assignment of the human alpha-tropomyosin gene TPM4 to band 19p13.1 by fluorescence in situ hybridizationS D Wilton, L Lim, S D Dorosz, et al.
The Medical Journal of Australia|July 15, 1996
Alzheimer's disease and apolipoprotein E genotype in Western Australia: an autopsy-verified seriesV A Fabian, T M Jones, S D Wilton, et al.
Genomics|August 1, 1992
A (CA)n repeat polymorphism for the human skeletal muscle alpha-actinin gene ACTN2 and its localization on the linkage map of chromosome 1A H Beggs, H A Phillips, H Kozman, et al.
Neuromuscular Disorders : NMD|August 22, 2006
Induced dystrophin exon skipping in human muscle explantsG McClorey, A M Fall, H M Moulton, et al.
Muscle & Nerve|July 9, 1998
Alternative dystrophin gene transcripts in golden retriever muscular dystrophyS J Schatzberg, L V Anderson, S D Wilton, et al.
Cytogenetics and Cell Genetics|January 1, 1994
Assignment of the human skeletal muscle alpha actin gene (ACTA1) to 1q42 by fluorescence in situ hybridisationP A Akkari, H J Eyre, S D Wilton, et al.
Oncogenesis|November 10, 2015
A novel BRD4-NUT fusion in an undifferentiated sinonasal tumor highlights alternative splicing as a contributing oncogenic factor in NUT midline carcinomaA Stirnweiss, K McCarthy, J Oommen, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 20, 2000
Antisense-induced exon skipping and synthesis of dystrophin in the mdx mouseC J Mann, K Honeyman, A J Cheng, et al.
Pageof 6

Showing results (31-40 of 52) with videos related to

Sort By:
Pageof 6
Cytogenetics and Cell Genetics|January 1, 1993
Assignment of the human slow skeletal muscle troponin gene (TNNI1) to 1q32 by fluorescence in situ hybridisationH J Eyre, P A Akkari, C Meredith, et al.
Neuromuscular Disorders : NMD|January 5, 2000
Homozygosity for a nonsense mutation in the alpha-tropomyosin slow gene TPM3 in a patient with severe infantile nemaline myopathyP Tan, J Briner, E Boltshauser, et al.
Cytogenetics and Cell Genetics|January 1, 1996
Assignment of the human alpha-tropomyosin gene TPM4 to band 19p13.1 by fluorescence in situ hybridizationS D Wilton, L Lim, S D Dorosz, et al.
The Medical Journal of Australia|July 15, 1996
Alzheimer's disease and apolipoprotein E genotype in Western Australia: an autopsy-verified seriesV A Fabian, T M Jones, S D Wilton, et al.
Genomics|August 1, 1992
A (CA)n repeat polymorphism for the human skeletal muscle alpha-actinin gene ACTN2 and its localization on the linkage map of chromosome 1A H Beggs, H A Phillips, H Kozman, et al.
Neuromuscular Disorders : NMD|August 22, 2006
Induced dystrophin exon skipping in human muscle explantsG McClorey, A M Fall, H M Moulton, et al.
Muscle & Nerve|July 9, 1998
Alternative dystrophin gene transcripts in golden retriever muscular dystrophyS J Schatzberg, L V Anderson, S D Wilton, et al.
Cytogenetics and Cell Genetics|January 1, 1994
Assignment of the human skeletal muscle alpha actin gene (ACTA1) to 1q42 by fluorescence in situ hybridisationP A Akkari, H J Eyre, S D Wilton, et al.
Oncogenesis|November 10, 2015
A novel BRD4-NUT fusion in an undifferentiated sinonasal tumor highlights alternative splicing as a contributing oncogenic factor in NUT midline carcinomaA Stirnweiss, K McCarthy, J Oommen, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 20, 2000
Antisense-induced exon skipping and synthesis of dystrophin in the mdx mouseC J Mann, K Honeyman, A J Cheng, et al.
Pageof 6