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D E Barton

Showing results (51-60 of 65) with videos related to

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Human Molecular Genetics|April 1, 1994
Direct, non-radioactive detection of mutations in multiple endocrine neoplasia type 2A familiesR McMahon, L M Mulligan, C S Healey, et al.
The Journal of Investigative Dermatology|November 1, 1989
Isolation, chromosomal mapping, and expression of the mouse tyrosinase geneB S Kwon, A K Haq, M Wakulchik, et al.
Molecular Genetics & Genomic Medicine|February 6, 2014
A new genome scan for primary nonsyndromic vesicoureteric reflux emphasizes high genetic heterogeneity and shows linkage and association with various genes already implicated in urinary tract developmentJ M Darlow, M G Dobson, R Darlay, et al.
Journal of Medical Genetics|December 1, 1992
Presymptomatic diagnosis of von Hippel-Lindau disease with flanking DNA markersE R Maher, E Bentley, S J Payne, et al.
Nature Genetics|August 1, 1994
Mutational bias provides a model for the evolution of Huntington's disease and predicts a general increase in disease prevalenceD C Rubinsztein, W Amos, J Leggo, et al.
Journal of Medical Genetics|May 1, 1995
Genetic linkage analysis in hereditary non-polyposis colon cancer syndromeN J Froggatt, J Koch, R Davies, et al.
Neurology|November 4, 2000
Rapid-onset dystonia-parkinsonism: a clinical and genetic analysis of a new kindredS J Pittock, C Joyce, V O'Keane, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|March 22, 2003
Predictive testing for BRCA1 and 2 mutations: a male contributionP A Daly, C Nolan, A Green, et al.
Archives of Disease in Childhood|April 1, 1993
Cystic fibrosis identified by neonatal screening: incidence, genotype, and early natural historyM R Green, L T Weaver, A F Heeley, et al.
Journal of Medical Genetics|August 1, 1993
Evaluation of molecular genetic diagnosis in the management of familial adenomatous polyposis coli: a population based studyE R Maher, D E Barton, R Slatter, et al.
Pageof 7

Showing results (51-60 of 65) with videos related to

Sort By:
Pageof 7
Human Molecular Genetics|April 1, 1994
Direct, non-radioactive detection of mutations in multiple endocrine neoplasia type 2A familiesR McMahon, L M Mulligan, C S Healey, et al.
The Journal of Investigative Dermatology|November 1, 1989
Isolation, chromosomal mapping, and expression of the mouse tyrosinase geneB S Kwon, A K Haq, M Wakulchik, et al.
Molecular Genetics & Genomic Medicine|February 6, 2014
A new genome scan for primary nonsyndromic vesicoureteric reflux emphasizes high genetic heterogeneity and shows linkage and association with various genes already implicated in urinary tract developmentJ M Darlow, M G Dobson, R Darlay, et al.
Journal of Medical Genetics|December 1, 1992
Presymptomatic diagnosis of von Hippel-Lindau disease with flanking DNA markersE R Maher, E Bentley, S J Payne, et al.
Nature Genetics|August 1, 1994
Mutational bias provides a model for the evolution of Huntington's disease and predicts a general increase in disease prevalenceD C Rubinsztein, W Amos, J Leggo, et al.
Journal of Medical Genetics|May 1, 1995
Genetic linkage analysis in hereditary non-polyposis colon cancer syndromeN J Froggatt, J Koch, R Davies, et al.
Neurology|November 4, 2000
Rapid-onset dystonia-parkinsonism: a clinical and genetic analysis of a new kindredS J Pittock, C Joyce, V O'Keane, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|March 22, 2003
Predictive testing for BRCA1 and 2 mutations: a male contributionP A Daly, C Nolan, A Green, et al.
Archives of Disease in Childhood|April 1, 1993
Cystic fibrosis identified by neonatal screening: incidence, genotype, and early natural historyM R Green, L T Weaver, A F Heeley, et al.
Journal of Medical Genetics|August 1, 1993
Evaluation of molecular genetic diagnosis in the management of familial adenomatous polyposis coli: a population based studyE R Maher, D E Barton, R Slatter, et al.
Pageof 7