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Genomics|November 1, 1992
Genetic heterogeneity in X-linked amelogenesis imperfectaM J Aldred, P J Crawford, E Roberts, et al.Human Genetics|December 1, 1988
Segregation of linked probes to myotonic dystrophy in a family demonstrating that 152 and APOC2 are on the same side of DM on 19qK Johnson, E Nimmo, P Jones, et al.Journal of Medical Genetics|November 1, 1991
Watson syndrome: is it a subtype of type 1 neurofibromatosis?J E Allanson, M Upadhyaya, G H Watson, et al.American Journal of Human Genetics|March 1, 1989
Evidence from family studies that the gene causing Huntington disease is telomeric to D4S95 and D4S90C Robbins, J Theilmann, S Youngman, et al.British Medical Journal (Clinical Research Ed.)|November 22, 1986
Application of a closely linked polymorphism of restriction fragment length to counselling and prenatal testing in families with myotonic dystrophyA L Meredith, S M Huson, P W Lunt, et al.Brain Research. Molecular Brain Research|June 3, 1999
Localization of rabbit huntingtin using a new panel of monoclonal antibodiesF L Wilkinson, T M Nguyen, S B Manilal, et al.Journal of Medical Genetics|December 1, 1992
Severity of chest disease in cystic fibrosis patients in relation to their genotypesL N al-Jader, A L Meredith, H C Ryley, et al.Human Molecular Genetics|July 1, 1993
Molecular analysis of British facioscapulohumeral dystrophy families for 4q DNA rearrangementsM Upadhyaya, P Jardine, J Maynard, et al.Human Genetics|November 1, 1986
Linkage relationships of the insulin receptor gene with the complement component 3, LDL receptor, apolipoprotein C2 and myotonic dystrophy loci on chromosome 19D J Shaw, A L Meredith, J D Brook, et al.Clinical Genetics|March 1, 1997
Carrier screening for cystic fibrosis in primary care: evaluation of a project in South Wales. The South Wales Cystic Fibrosis Carrier Screening Research TeamY Payne, M Williams, J Cheadle, et al.Pageof 23