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D E Barton

Showing results (31-40 of 65) with videos related to

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Journal of Medical Genetics|November 1, 1996
Improved genetic mapping of X linked retinoschisisN D George, S J Payne, R M Bill, et al.
Human Molecular Genetics|February 1, 1994
Somatic NF2 gene mutations in familial and non-familial vestibular schwannomaR M Irving, D A Moffat, D G Hardy, et al.
Journal of Medical Genetics|October 1, 1994
Mosaic uniparental disomy in Beckwith-Wiedemann syndromeR E Slatter, M Elliott, K Welham, et al.
Clinical Genetics|April 1, 1993
Genotype analysis in cystic fibrosis in relation to the occurrence of diabetes mellitusI Hamdi, S J Payne, D E Barton, et al.
Archives of Otolaryngology--Head & Neck Surgery|November 1, 1993
Molecular genetic analysis of the mechanism of tumorigenesis in acoustic neuromaR M Irving, D A Moffat, D G Hardy, et al.
Journal of Medical Genetics|November 1, 1993
Genetic mapping of the Kallmann syndrome and X linked ocular albinism gene lociY Zhang, R McMahon, S J Charles, et al.
Clinical Genetics|December 1, 1995
Molecular genetic analysis of exons 1 to 6 of the APC gene in non-polyposis familial colorectal cancerJ A Joyce, N J Froggatt, R Davies, et al.
Archives of Disease in Childhood|April 8, 1999
Hyperinsulinism: molecular aetiology of focal diseaseF Ryan, D Devaney, C Joyce, et al.
Diabetes|July 30, 1999
Hyperinsulinism caused by paternal-specific inheritance of a recessive mutation in the sulfonylurea-receptor geneB Glaser, F Ryan, M Donath, et al.
Journal of Neurosurgery|May 1, 1996
Molecular genetic investigation of the neurofibromatosis type 2 tumor suppressor gene in sporadic meningiomaT Harada, R M Irving, J H Xuereb, et al.
Pageof 7

Showing results (31-40 of 65) with videos related to

Sort By:
Pageof 7
Journal of Medical Genetics|November 1, 1996
Improved genetic mapping of X linked retinoschisisN D George, S J Payne, R M Bill, et al.
Human Molecular Genetics|February 1, 1994
Somatic NF2 gene mutations in familial and non-familial vestibular schwannomaR M Irving, D A Moffat, D G Hardy, et al.
Journal of Medical Genetics|October 1, 1994
Mosaic uniparental disomy in Beckwith-Wiedemann syndromeR E Slatter, M Elliott, K Welham, et al.
Clinical Genetics|April 1, 1993
Genotype analysis in cystic fibrosis in relation to the occurrence of diabetes mellitusI Hamdi, S J Payne, D E Barton, et al.
Archives of Otolaryngology--Head & Neck Surgery|November 1, 1993
Molecular genetic analysis of the mechanism of tumorigenesis in acoustic neuromaR M Irving, D A Moffat, D G Hardy, et al.
Journal of Medical Genetics|November 1, 1993
Genetic mapping of the Kallmann syndrome and X linked ocular albinism gene lociY Zhang, R McMahon, S J Charles, et al.
Clinical Genetics|December 1, 1995
Molecular genetic analysis of exons 1 to 6 of the APC gene in non-polyposis familial colorectal cancerJ A Joyce, N J Froggatt, R Davies, et al.
Archives of Disease in Childhood|April 8, 1999
Hyperinsulinism: molecular aetiology of focal diseaseF Ryan, D Devaney, C Joyce, et al.
Diabetes|July 30, 1999
Hyperinsulinism caused by paternal-specific inheritance of a recessive mutation in the sulfonylurea-receptor geneB Glaser, F Ryan, M Donath, et al.
Journal of Neurosurgery|May 1, 1996
Molecular genetic investigation of the neurofibromatosis type 2 tumor suppressor gene in sporadic meningiomaT Harada, R M Irving, J H Xuereb, et al.
Pageof 7