Showing results (71-80 of 220) with videos related to
Sort By:
Pageof 22
Genomics|August 1, 1992
Determination of the exon structure of the distal portion of the dystrophin gene by vectorette PCRR G Roberts, A J Coffey, M Bobrow, et al.British Journal of Diseases of the Chest|July 1, 1983
HLA-A, B and DR antigens and properdin factor B allotypes in Caplan's syndromeC Darke, M M Wagner, G Nuki, et al.Nucleic Acids Research|August 11, 1989
Detection of novel genetic markers by mismatch analysisR G Roberts, A J Montandon, M Bobrow, et al.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.Pageof 22