|
Samson, F; Mesnard, L; Mihovilovic, M et al. (1994) A new human slow skeletal troponin T (TnTs) mRNA isoform derived from alternative splicing of a single gene. Biochem Biophys Res Commun 199:841-7
|
|
Roses, A D (1993) Molecular genetics of neurodegenerative diseases. Curr Opin Neurol Neurosurg 6:34-9
|
|
Speer, M C; Yamaoka, L H; Gilchrist, J H et al. (1992) Confirmation of genetic heterogeneity in limb-girdle muscular dystrophy: linkage of an autosomal dominant form to chromosome 5q. Am J Hum Genet 50:1211-7
|
|
Kazantsev, A; Yamaoka, L H; Roses, A D (1992) A dinucleotide repeat polymorphism in the human Na+,K+ ATPase, alpha subunit (ATP1A3) gene. Nucleic Acids Res 20:1164
|
|
Samson, F; de Jong, P J; Trask, B J et al. (1992) Assignment of the human slow skeletal troponin T gene to 19q13.4 using somatic cell hybrids and fluorescence in situ hybridization analysis. Genomics 13:1374-5
|
|
Gilbert, J R; Stajich, J M; Speer, M C et al. (1992) Linkage studies in facioscapulohumeral muscular dystrophy (FSHD). Am J Hum Genet 51:424-7
|
|
Samson, F; Gilbert, J R; Koza-Taylor, P et al. (1991) A PstI polymorphism detected by a genomic clone at the human slow troponin T (TNNT1) gene locus. Nucleic Acids Res 19:6058
|
|
Secore, S L; Walker, A P; Herbstreith, M H et al. (1991) A StuI polymorphism on chromosome 3p14.1-14.2 (D3S622) defined by two polymorphic StuI sites 2.4 kb apart. Nucleic Acids Res 19:6349
|
|
Speer, M C; Pericak-Vance, M A; Yamaoka, L et al. (1990) Presymptomatic and prenatal diagnosis in myotonic dystrophy by genetic linkage studies. Neurology 40:671-6
|
|
Roses, A D; Pericak-Vance, M A; Clark, C M et al. (1990) Linkage studies of late-onset familial Alzheimer's disease. Adv Neurol 51:185-96
|
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