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Pediatric Nephrology (Berlin, Germany)|July 1, 1988
The application of molecular biology to the prenatal diagnosis of renal diseaseF A Flinter, M BobrowGenomics|April 1, 1989
Localization of the gene for classic Alport syndromeF A Flinter, S Abbs, M BobrowLancet (London, England)|October 29, 1988
Genetics of classic Alport's syndromeF A Flinter, J S Cameron, C Chantler, et al.Human Genetics|August 1, 1992
A novel NcoI polymorphism creates a fifth haplotype in the 3' untranslated region of CKMA M Differ, M Bobrow, C G MathewJournal of Medical Genetics|March 1, 1995
A rapid, non-radioactive screening test for fragile X mutations at the FRAXA and FRAXE lociQ Wang, E Green, 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.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 1, 1991
A convenient multiplex PCR system for the detection of dystrophin gene deletions: a comparative analysis with cDNA hybridisation shows mistypings by both methodsS Abbs, S C Yau, S Clark, et al.Genomics|August 1, 1990
Accurate assessment of intragenic recombination frequency within the Duchenne muscular dystrophy geneS Abbs, R G Roberts, C G Mathew, et al.Lancet (London, England)|October 23, 1993
Cytogenetic versus DNA diagnosis in routine referrals for fragile X syndromeQ Wang, E Green, A Barnicoat, et al.Pageof 125