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D L Thiselton

Showing results (11-20 of 23) with videos related to

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Human Mutation|June 22, 2000
Novel frameshift mutations in the RP2 gene and polymorphic variantsD L Thiselton, I Zito, C Plant, et al.
Human Genetics|September 10, 1999
Identification of novel RPGR (retinitis pigmentosa GTPase regulator) mutations in a subset of X-linked retinitis pigmentosa families segregating with the RP3 locusI Zito, D L Thiselton, M B Gorin, et al.
Human Genetics|December 6, 2001
A frameshift mutation in exon 28 of the OPA1 gene explains the high prevalence of dominant optic atrophy in the Danish population: evidence for a founder effectD L Thiselton, C Alexander, A Morris, et al.
Human Genetics|January 1, 1992
Localisation of the gene for Norrie disease to between DXS7 and DXS426 on XpS Lindsay, D L Thiselton, J B Bateman, et al.
Genome Research|November 1, 1996
Mapping the RP2 locus for X-linked retinitis pigmentosa on proximal Xp: a genetically defined 5-cM critical region and exclusion of candidate genes by physical mappingD L Thiselton, R M Hampson, M Nayudu, et al.
Molecular Psychiatry|June 16, 2004
No evidence for linkage or association of neuregulin-1 (NRG1) with disease in the Irish study of high-density schizophrenia families (ISHDSF)D L Thiselton, B T Webb, B M Neale, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 29, 2009
Association analysis of the PIP4K2A gene on chromosome 10p12 and schizophrenia in the Irish study of high density schizophrenia families (ISHDSF) and the Irish case-control study of schizophrenia (ICCSS)D L Thiselton, B S Maher, B T Webb, et al.
American Journal of Human Genetics|March 26, 1999
Mutations in the RP2 gene cause disease in 10% of families with familial X-linked retinitis pigmentosa assessed in this studyA J Hardcastle, D L Thiselton, L Van Maldergem, et al.
Nature Genetics|October 4, 2000
OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28C Alexander, M Votruba, U E Pesch, et al.
Molecular Psychiatry|May 17, 2007
A region of 35 kb containing the trace amine associate receptor 6 (TAAR6) gene is associated with schizophrenia in the Irish study of high-density schizophrenia familiesV Vladimirov, D L Thiselton, P-H Kuo, et al.
Pageof 3

Showing results (11-20 of 23) with videos related to

Sort By:
Pageof 3
Human Mutation|June 22, 2000
Novel frameshift mutations in the RP2 gene and polymorphic variantsD L Thiselton, I Zito, C Plant, et al.
Human Genetics|September 10, 1999
Identification of novel RPGR (retinitis pigmentosa GTPase regulator) mutations in a subset of X-linked retinitis pigmentosa families segregating with the RP3 locusI Zito, D L Thiselton, M B Gorin, et al.
Human Genetics|December 6, 2001
A frameshift mutation in exon 28 of the OPA1 gene explains the high prevalence of dominant optic atrophy in the Danish population: evidence for a founder effectD L Thiselton, C Alexander, A Morris, et al.
Human Genetics|January 1, 1992
Localisation of the gene for Norrie disease to between DXS7 and DXS426 on XpS Lindsay, D L Thiselton, J B Bateman, et al.
Genome Research|November 1, 1996
Mapping the RP2 locus for X-linked retinitis pigmentosa on proximal Xp: a genetically defined 5-cM critical region and exclusion of candidate genes by physical mappingD L Thiselton, R M Hampson, M Nayudu, et al.
Molecular Psychiatry|June 16, 2004
No evidence for linkage or association of neuregulin-1 (NRG1) with disease in the Irish study of high-density schizophrenia families (ISHDSF)D L Thiselton, B T Webb, B M Neale, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 29, 2009
Association analysis of the PIP4K2A gene on chromosome 10p12 and schizophrenia in the Irish study of high density schizophrenia families (ISHDSF) and the Irish case-control study of schizophrenia (ICCSS)D L Thiselton, B S Maher, B T Webb, et al.
American Journal of Human Genetics|March 26, 1999
Mutations in the RP2 gene cause disease in 10% of families with familial X-linked retinitis pigmentosa assessed in this studyA J Hardcastle, D L Thiselton, L Van Maldergem, et al.
Nature Genetics|October 4, 2000
OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28C Alexander, M Votruba, U E Pesch, et al.
Molecular Psychiatry|May 17, 2007
A region of 35 kb containing the trace amine associate receptor 6 (TAAR6) gene is associated with schizophrenia in the Irish study of high-density schizophrenia familiesV Vladimirov, D L Thiselton, P-H Kuo, et al.
Pageof 3