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M Bobrow

Showing results (131-140 of 235) with videos related to

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Journal of Medical Genetics|May 5, 1999
Identification and quantification of somatic mosaicism for a point mutation in a Duchenne muscular dystrophy familyT A Smith, S C Yau, M Bobrow, et al.
Genomics|May 1, 1993
Exon structure of the human dystrophin geneR G Roberts, A J Coffey, M Bobrow, et al.
Patient Education and Counseling|November 14, 1997
Information recall in genetic counselling: a pilot study of its assessmentS Michie, D French, A Allanson, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|April 15, 2000
Detailed analysis of the oligodendrocyte myelin glycoprotein gene in four patients with neurofibromatosis 1 and primary progressive multiple sclerosisM R Johnson, R E Ferner, M Bobrow, et al.
American Journal of Diseases of Children (1960)|August 1, 1973
Ring-1 chromosome, microcephalic dwarfism, and acute myeloid leukemiaM Bobrow, P M Emerson, A I Spriggs, et al.
Journal of Medical Genetics|February 1, 1992
Fertility in a male with trisomy 21M Bobrow, T Barby, A Hajianpour, et al.
Genomics|July 1, 1991
Generation of novel sequence tagged sites (STSs) from discrete chromosomal regions using Alu-PCRC G Cole, P N Goodfellow, M Bobrow, et al.
Journal of Medical Genetics|February 1, 1991
Tay-Sachs disease heterozygote detection: use of a centrifugal analyser for automation of hexosaminidase assays with two different artificial substratesE C Landels, I H Ellis, M Bobrow, et al.
Human Genetics|September 1, 1987
A small deletion in the Duchenne/Becker muscular dystrophy locus--a functionally important region?K A Hart, A P Monaco, L M Kunkel, et al.
Health Technology Assessment (Winchester, England)|March 23, 2001
An assessment of screening strategies for fragile X syndrome in the UKM E Pembrey, A J Barnicoat, B Carmichael, et al.
Pageof 24

Showing results (131-140 of 235) with videos related to

Sort By:
Pageof 24
Journal of Medical Genetics|May 5, 1999
Identification and quantification of somatic mosaicism for a point mutation in a Duchenne muscular dystrophy familyT A Smith, S C Yau, M Bobrow, et al.
Genomics|May 1, 1993
Exon structure of the human dystrophin geneR G Roberts, A J Coffey, M Bobrow, et al.
Patient Education and Counseling|November 14, 1997
Information recall in genetic counselling: a pilot study of its assessmentS Michie, D French, A Allanson, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|April 15, 2000
Detailed analysis of the oligodendrocyte myelin glycoprotein gene in four patients with neurofibromatosis 1 and primary progressive multiple sclerosisM R Johnson, R E Ferner, M Bobrow, et al.
American Journal of Diseases of Children (1960)|August 1, 1973
Ring-1 chromosome, microcephalic dwarfism, and acute myeloid leukemiaM Bobrow, P M Emerson, A I Spriggs, et al.
Journal of Medical Genetics|February 1, 1992
Fertility in a male with trisomy 21M Bobrow, T Barby, A Hajianpour, et al.
Genomics|July 1, 1991
Generation of novel sequence tagged sites (STSs) from discrete chromosomal regions using Alu-PCRC G Cole, P N Goodfellow, M Bobrow, et al.
Journal of Medical Genetics|February 1, 1991
Tay-Sachs disease heterozygote detection: use of a centrifugal analyser for automation of hexosaminidase assays with two different artificial substratesE C Landels, I H Ellis, M Bobrow, et al.
Human Genetics|September 1, 1987
A small deletion in the Duchenne/Becker muscular dystrophy locus--a functionally important region?K A Hart, A P Monaco, L M Kunkel, et al.
Health Technology Assessment (Winchester, England)|March 23, 2001
An assessment of screening strategies for fragile X syndrome in the UKM E Pembrey, A J Barnicoat, B Carmichael, et al.
Pageof 24