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Journal of Medical Genetics|August 1, 1983
Linkage analysis of myotonic dystrophy and sequences on chromosome 19 using a cloned complement 3 gene probeK E Davies, J Jackson, R Williamson, et al.Journal of Medical Genetics|November 1, 1992
Specific molecular prenatal diagnosis for the CTG mutation in myotonic dystrophyJ Myring, A L Meredith, H G Harley, et al.Journal of Medical Genetics|April 1, 1991
Paternal origin of the chromosomal deletion resulting in Wolf-Hirschhorn syndromeO W Quarrell, R G Snell, M A Curtis, et al.Annals of the New York Academy of Sciences|January 1, 1986
Evidence against linkage of von Recklinghausen neurofibromatosis and chromosome 19 markersS M Huson, A L Meredith, M Sarfarazi, et al.Archives of Disease in Childhood|September 1, 1994
De novo facioscapulohumeral muscular dystrophy defined by DNA probe p13E-11 (D4F104S1)P E Jardine, M C Koch, P W Lunt, et al.Muscle & Nerve. Supplement|January 1, 1995
Phenotypic-genotypic correlation will assist genetic counseling in 4q35-facioscapulohumeral muscular dystrophyP W Lunt, P E Jardine, M Koch, et al.Human Molecular Genetics|August 11, 1999
Aberrant interactions of transcriptional repressor proteins with the Huntington's disease gene product, huntingtinJ M Boutell, P Thomas, J W Neal, et al.Muscle & Nerve. Supplement|April 12, 2013
Phenotypic-genotypic correlation will assist genetic counseling in 4q35-facioscapulohumeral muscular dystrophyP W Lunt, P E Jardine, M Koch, et al.Journal of Medical Genetics|March 1, 1993
A study of DNA methylation in myotonic dystrophyD J Shaw, S Chaudhary, S A Rundle, et al.Human Genetics|January 1, 1985
The apolipoprotein CII gene: subchromosomal localisation and linkage to the myotonic dystrophy locusD J Shaw, A L Meredith, M Sarfarazi, et al.Pageof 23