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R G Snell

Showing results (11-20 of 43) with videos related to

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Neuroscience|May 27, 2005
TATA-binding protein in neurodegenerative diseaseW M C van Roon-Mom, S J Reid, R L M Faull, et al.
Human Genetics|April 4, 2000
Further evidence of autosomal dominant congenital zonular pulverulent cataracts linked to 13q11 (CZP3) and a novel mutation in connexin 46 (GJA3)M I Rees, P Watts, I Fenton, et al.
Journal of Medical Genetics|August 1, 1991
Linkage disequilibrium and recombination make a telomeric site for the Huntington's disease gene unlikelyL Barron, A Curtis, A E Shrimpton, et al.
Neuroscience|January 22, 2003
Distribution of gephyrin in the human brain: an immunohistochemical analysisH J Waldvogel, K Baer, R G Snell, et al.
Brain Research|April 24, 2018
Emergence of breath testing as a new non-invasive diagnostic modality for neurodegenerative diseasesN Siva Subramaniam, C S Bawden, H Waldvogel, et al.
Journal of Medical Genetics|April 1, 1991
Paternal origin of the chromosomal deletion resulting in Wolf-Hirschhorn syndromeO W Quarrell, R G Snell, M A Curtis, et al.
Nucleic Acids Research|October 11, 1991
MboI RFLP at the D4S43 (C4H) locusL P Lazarou, R G Snell, M E MacDonald, et al.
Neuroscience|November 19, 2003
Association of gephyrin and glycine receptors in the human brainstem and spinal cord: an immunohistochemical analysisK Baer, H J Waldvogel, M J During, et al.
Gene|November 14, 1997
Structure and sequence of the bovine butyrophilin geneH W Davey, S L Ogg, Y Husaini, et al.
Journal of Medical Genetics|November 1, 1989
Linkage disequilibrium in Huntington's disease: an improved localisation for the geneR G Snell, L P Lazarou, S Youngman, et al.
Pageof 5

Showing results (11-20 of 43) with videos related to

Sort By:
Pageof 5
Neuroscience|May 27, 2005
TATA-binding protein in neurodegenerative diseaseW M C van Roon-Mom, S J Reid, R L M Faull, et al.
Human Genetics|April 4, 2000
Further evidence of autosomal dominant congenital zonular pulverulent cataracts linked to 13q11 (CZP3) and a novel mutation in connexin 46 (GJA3)M I Rees, P Watts, I Fenton, et al.
Journal of Medical Genetics|August 1, 1991
Linkage disequilibrium and recombination make a telomeric site for the Huntington's disease gene unlikelyL Barron, A Curtis, A E Shrimpton, et al.
Neuroscience|January 22, 2003
Distribution of gephyrin in the human brain: an immunohistochemical analysisH J Waldvogel, K Baer, R G Snell, et al.
Brain Research|April 24, 2018
Emergence of breath testing as a new non-invasive diagnostic modality for neurodegenerative diseasesN Siva Subramaniam, C S Bawden, H Waldvogel, et al.
Journal of Medical Genetics|April 1, 1991
Paternal origin of the chromosomal deletion resulting in Wolf-Hirschhorn syndromeO W Quarrell, R G Snell, M A Curtis, et al.
Nucleic Acids Research|October 11, 1991
MboI RFLP at the D4S43 (C4H) locusL P Lazarou, R G Snell, M E MacDonald, et al.
Neuroscience|November 19, 2003
Association of gephyrin and glycine receptors in the human brainstem and spinal cord: an immunohistochemical analysisK Baer, H J Waldvogel, M J During, et al.
Gene|November 14, 1997
Structure and sequence of the bovine butyrophilin geneH W Davey, S L Ogg, Y Husaini, et al.
Journal of Medical Genetics|November 1, 1989
Linkage disequilibrium in Huntington's disease: an improved localisation for the geneR G Snell, L P Lazarou, S Youngman, et al.
Pageof 5