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P Tarpey

Showing results (1-10 of 13) with videos related to

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Human Mutation|November 3, 2000
Comparative sequence analysis (CSA): a new sequence-based method for the identification and characterization of mutations in DNAC Mattocks, P Tarpey, M Bobrow, et al.
Journal of Clinical Pathology|November 1, 1980
IgM associated primary diffuse mesangial proliferative glomerulonephritisW Lawler, G Williams, P Tarpey, et al.
Journal of Clinical Pathology|October 1, 1977
IgA localisation in glomerular diseasesW Lawler, G Williams, P Tarpey, et al.
Journal of Clinical Pathology|May 1, 1976
Diseases and histological normality of the renal glomerulus: a clinicopathological studyW Lawler, P Tarpey, G Williams, et al.
Journal of Medical Genetics|April 3, 2004
Automated comparative sequence analysis identifies mutations in 89% of NF1 patients and confirms a mutation cluster in exons 11-17 distinct from the GAP related domainC Mattocks, D Baralle, P Tarpey, et al.
Journal of Medical Genetics|June 7, 2005
Re: Pitfalls of automated comparative sequence analysis as a single platform for routine clinical testing for NF1 (Messiaen and Wimmer)J L Whittaker, C Mattocks, D Baralle, et al.
Journal of Medical Genetics|July 5, 2005
Re: Pitfalls of automated comparative sequence analysis as a single platform for routine clinical testing for NF1 (Messiaen and Wimmer)J L Whittaker, C Mattocks, D Baralle, et al.
American Journal of Medical Genetics|August 15, 2001
De novo deletion of chromosome 18q in a baby with harlequin ichthyosisH Stewart, P T Smith, L Gaunt, et al.
Frontiers in Genetics|December 7, 2020
Mastermind: A Comprehensive Genomic Association Search Engine for Empirical Evidence Curation and Genetic Variant InterpretationLauren M Chunn, Diane C Nefcy, Rachel W Scouten, et al.
Clinical Genetics|November 15, 2006
Mutations in the RSK2(RPS6KA3) gene cause Coffin-Lowry syndrome and nonsyndromic X-linked mental retardationM Field, P Tarpey, J Boyle, et al.
Pageof 2

Showing results (1-10 of 13) with videos related to

Sort By:
Pageof 2
Human Mutation|November 3, 2000
Comparative sequence analysis (CSA): a new sequence-based method for the identification and characterization of mutations in DNAC Mattocks, P Tarpey, M Bobrow, et al.
Journal of Clinical Pathology|November 1, 1980
IgM associated primary diffuse mesangial proliferative glomerulonephritisW Lawler, G Williams, P Tarpey, et al.
Journal of Clinical Pathology|October 1, 1977
IgA localisation in glomerular diseasesW Lawler, G Williams, P Tarpey, et al.
Journal of Clinical Pathology|May 1, 1976
Diseases and histological normality of the renal glomerulus: a clinicopathological studyW Lawler, P Tarpey, G Williams, et al.
Journal of Medical Genetics|April 3, 2004
Automated comparative sequence analysis identifies mutations in 89% of NF1 patients and confirms a mutation cluster in exons 11-17 distinct from the GAP related domainC Mattocks, D Baralle, P Tarpey, et al.
Journal of Medical Genetics|June 7, 2005
Re: Pitfalls of automated comparative sequence analysis as a single platform for routine clinical testing for NF1 (Messiaen and Wimmer)J L Whittaker, C Mattocks, D Baralle, et al.
Journal of Medical Genetics|July 5, 2005
Re: Pitfalls of automated comparative sequence analysis as a single platform for routine clinical testing for NF1 (Messiaen and Wimmer)J L Whittaker, C Mattocks, D Baralle, et al.
American Journal of Medical Genetics|August 15, 2001
De novo deletion of chromosome 18q in a baby with harlequin ichthyosisH Stewart, P T Smith, L Gaunt, et al.
Frontiers in Genetics|December 7, 2020
Mastermind: A Comprehensive Genomic Association Search Engine for Empirical Evidence Curation and Genetic Variant InterpretationLauren M Chunn, Diane C Nefcy, Rachel W Scouten, et al.
Clinical Genetics|November 15, 2006
Mutations in the RSK2(RPS6KA3) gene cause Coffin-Lowry syndrome and nonsyndromic X-linked mental retardationM Field, P Tarpey, J Boyle, et al.
Pageof 2