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Lancet (London, England)|January 30, 1993
Direct diagnosis of carriers of point mutations in Duchenne muscular dystrophyS C Yau, R G Roberts, M Bobrow, et al.Cytogenetics and Cell Genetics|January 1, 1983
Nucleoli, micronucleoli, and nucleolus-like structures in human oocytes at meiotic prophase I studied by the silver-NOR techniqueM Hartung, J W Keeling, C Patel, et al.Journal of Medical Genetics|July 1, 1996
Accurate diagnosis of carriers of deletions and duplications in Duchenne/Becker muscular dystrophy by fluorescent dosage analysisS C Yau, M Bobrow, C G Mathew, et al.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.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.Pageof 423