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R F Mueller

Showing results (41-50 of 85) with videos related to

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Lancet (London, England)|August 19, 1989
Hypervariable microsatellite for genetic diagnosisG R Taylor, J S Noble, J L Hall, et al.
Disease Markers|November 1, 1991
A rapid PCR-based method to distinguish between fetal and maternal cells in chorionic biopsies using microsatellite polymorphismsJ S Noble, G R Taylor, A D Stewart, et al.
Audiology : Official Organ of the International Society of Audiology|August 30, 2000
Population-based genetic study of childhood hearing impairment in the Trent Region of the United KingdomM J Parker, H M Fortnum, I D Young, et al.
American Journal of Human Genetics|May 1, 1983
Plasma paraoxonase polymorphism: a new enzyme assay, population, family, biochemical, and linkage studiesR F Mueller, S Hornung, C E Furlong, et al.
Journal of Medical Genetics|April 3, 2001
Prevalence of mitochondrial DNA mutations in childhood/congenital onset non-syndromal sensorineural hearing impairmentT P Hutchin, K R Thompson, M Parker, et al.
Human Molecular Genetics|February 1, 1993
A novel insertional mutation at the third zinc finger coding region of the WT1 gene in Denys-Drash syndromeO Ogawa, M R Eccles, K Yun, et al.
Journal of Medical Genetics|June 1, 1992
The 3-M syndrome: risk of intracerebral aneurysm?R F Mueller, J Buckler, R Arthur, et al.
Journal of Medical Genetics|January 1, 1990
The Schinzel-Giedion syndromeL I al-Gazali, P Farndon, J Burn, et al.
Journal of Medical Genetics|November 10, 2000
Clinical phenotypes and molecular characterisation of three patients with Ehlers-Danlos syndrome type VIIA C Nicholls, J L Sher, M J Wright, et al.
Annals of Human Genetics|September 1, 1996
Human sequences homologous to the gene for the cochlear protein Ocp-II do not map to currently known non-syndromic hearing loss lociK A Brown, J P Leek, N J Lench, et al.
Pageof 9

Showing results (41-50 of 85) with videos related to

Sort By:
Pageof 9
Lancet (London, England)|August 19, 1989
Hypervariable microsatellite for genetic diagnosisG R Taylor, J S Noble, J L Hall, et al.
Disease Markers|November 1, 1991
A rapid PCR-based method to distinguish between fetal and maternal cells in chorionic biopsies using microsatellite polymorphismsJ S Noble, G R Taylor, A D Stewart, et al.
Audiology : Official Organ of the International Society of Audiology|August 30, 2000
Population-based genetic study of childhood hearing impairment in the Trent Region of the United KingdomM J Parker, H M Fortnum, I D Young, et al.
American Journal of Human Genetics|May 1, 1983
Plasma paraoxonase polymorphism: a new enzyme assay, population, family, biochemical, and linkage studiesR F Mueller, S Hornung, C E Furlong, et al.
Journal of Medical Genetics|April 3, 2001
Prevalence of mitochondrial DNA mutations in childhood/congenital onset non-syndromal sensorineural hearing impairmentT P Hutchin, K R Thompson, M Parker, et al.
Human Molecular Genetics|February 1, 1993
A novel insertional mutation at the third zinc finger coding region of the WT1 gene in Denys-Drash syndromeO Ogawa, M R Eccles, K Yun, et al.
Journal of Medical Genetics|June 1, 1992
The 3-M syndrome: risk of intracerebral aneurysm?R F Mueller, J Buckler, R Arthur, et al.
Journal of Medical Genetics|January 1, 1990
The Schinzel-Giedion syndromeL I al-Gazali, P Farndon, J Burn, et al.
Journal of Medical Genetics|November 10, 2000
Clinical phenotypes and molecular characterisation of three patients with Ehlers-Danlos syndrome type VIIA C Nicholls, J L Sher, M J Wright, et al.
Annals of Human Genetics|September 1, 1996
Human sequences homologous to the gene for the cochlear protein Ocp-II do not map to currently known non-syndromic hearing loss lociK A Brown, J P Leek, N J Lench, et al.
Pageof 9