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Showing results (201-210 of 235) with videos related to

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Neuromuscular Disorders : NMD|January 1, 1992
Linkage of Emery-Dreifuss muscular dystrophy to the red/green cone pigment (RGCP) genes, proximal to factor VIIIC G Cole, S J Abbs, V Dubowitz, et al.
Journal of Medical Genetics|March 1, 1989
Spontaneous and induced chromosome breakage in chorionic villus samples: a cytogenetic approach to first trimester prenatal diagnosis of ataxia telangiectasia syndromeJ Llerena, M Murer-Orlando, M McGuire, et al.
Lancet (London, England)|February 6, 1988
Prenatal testing for Duchenne and Becker muscular dystrophyC G Cole, A Walker, A Coyne, et al.
Journal of Medical Genetics|December 1, 1986
The screening of Duchenne muscular dystrophy patients for submicroscopic deletionsK Hart, C Cole, A Walker, et al.
Nature|March 20, 1975
The beta2-microglobulin gene is on chromosome 15 and not in the HL-A regionP N Goodfellow, E A Jones, V Van Heyningen, et al.
Annals of Human Genetics|May 1, 1976
Evidence for the assignment of the loci AK1, AK3 and ACONs to chromosome 9 in manS Povey, C A Slaughter, D E Wilson, et al.
Lancet (London, England)|August 8, 1981
Regional localisation of the human alpha-globin genesJ S Wainscoat, E Kanavakis, D J Weatherall, et al.
Human Molecular Genetics|February 1, 1993
The identification of a third fragile site, FRAXF, in Xq27--q28 distal to both FRAXA and FRAXEM C Hirst, A Barnicoat, G Flynn, et al.
Genomics|October 1, 1992
A random STS strategy for construction of YAC contigs spanning defined chromosomal regionsC G Cole, I Dunham, A J Coffey, et al.
British Journal of Obstetrics and Gynaecology|March 1, 1979
Clinical dilemmas arising from the antenatal diagnosis of neural tube defectsG M Stirrat, A C Turnbull, M J Bennett, et al.
Pageof 24

Showing results (201-210 of 235) with videos related to

Sort By:
Pageof 24
Neuromuscular Disorders : NMD|January 1, 1992
Linkage of Emery-Dreifuss muscular dystrophy to the red/green cone pigment (RGCP) genes, proximal to factor VIIIC G Cole, S J Abbs, V Dubowitz, et al.
Journal of Medical Genetics|March 1, 1989
Spontaneous and induced chromosome breakage in chorionic villus samples: a cytogenetic approach to first trimester prenatal diagnosis of ataxia telangiectasia syndromeJ Llerena, M Murer-Orlando, M McGuire, et al.
Lancet (London, England)|February 6, 1988
Prenatal testing for Duchenne and Becker muscular dystrophyC G Cole, A Walker, A Coyne, et al.
Journal of Medical Genetics|December 1, 1986
The screening of Duchenne muscular dystrophy patients for submicroscopic deletionsK Hart, C Cole, A Walker, et al.
Nature|March 20, 1975
The beta2-microglobulin gene is on chromosome 15 and not in the HL-A regionP N Goodfellow, E A Jones, V Van Heyningen, et al.
Annals of Human Genetics|May 1, 1976
Evidence for the assignment of the loci AK1, AK3 and ACONs to chromosome 9 in manS Povey, C A Slaughter, D E Wilson, et al.
Lancet (London, England)|August 8, 1981
Regional localisation of the human alpha-globin genesJ S Wainscoat, E Kanavakis, D J Weatherall, et al.
Human Molecular Genetics|February 1, 1993
The identification of a third fragile site, FRAXF, in Xq27--q28 distal to both FRAXA and FRAXEM C Hirst, A Barnicoat, G Flynn, et al.
Genomics|October 1, 1992
A random STS strategy for construction of YAC contigs spanning defined chromosomal regionsC G Cole, I Dunham, A J Coffey, et al.
British Journal of Obstetrics and Gynaecology|March 1, 1979
Clinical dilemmas arising from the antenatal diagnosis of neural tube defectsG M Stirrat, A C Turnbull, M J Bennett, et al.
Pageof 24