Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Clinical Investigator Award (CIA) (K08)
Project #
5K08NS001289-04
Application #
3084179
Study Section
Neurological Disorders Program Project Review B Committee (NSPB)
Project Start
1988-08-01
Project End
1993-07-31
Budget Start
1991-08-01
Budget End
1992-07-31
Support Year
4
Fiscal Year
1991
Total Cost
Indirect Cost
Name
Duke University
Department
Type
Schools of Medicine
DUNS #
071723621
City
Durham
State
NC
Country
United States
Zip Code
27705
Loeb, D; Lui, W; Smith, D I et al. (1994) Dinucleotide repeat polymorphism in the VHL region. Hum Mol Genet 3:520
Pericak-Vance, M A; Nunes, K J; Whisenant, E et al. (1993) Genetic mapping of dinucleotide repeat polymorphisms and von Hippel-Lindau disease on chromosome 3p25-26. J Med Genet 30:487-91
Ben Othmane, K; Middleton, L T; Loprest, L J et al. (1993) Localization of a gene (CMT2A) for autosomal dominant Charcot-Marie-Tooth disease type 2 to chromosome 1p and evidence of genetic heterogeneity. Genomics 17:370-5
Ben Othmane, K; Hentati, F; Lennon, F et al. (1993) Linkage of a locus (CMT4A) for autosomal recessive Charcot-Marie-Tooth disease to chromosome 8q. Hum Mol Genet 2:1625-8
Loeb, D; Lui, W; Smith, D I et al. (1993) Dinucleotide repeat polymorphisms in the VHL region of human chromosome 3p25. Hum Mol Genet 2:1746
Loprest, L J; Pericak-Vance, M A; Stajich, J et al. (1992) Linkage studies in Charcot-Marie-Tooth disease type 2: evidence that CMT types 1 and 2 are distinct genetic entities. Neurology 42:597-601
Vance, J M (1991) Hereditary motor and sensory neuropathies. J Med Genet 28:1-5
Vance, J M; Barker, D; Yamaoka, L H et al. (1991) Localization of Charcot-Marie-Tooth disease type 1a (CMT1A) to chromosome 17p11.2. Genomics 9:623-8
Lucas, A M; Vance, J M; Stajich, J M et al. (1991) A PvuII polymorphism detected by pEW404 (D17S64) on chromosome 17. Nucleic Acids Res 19:5802
Vance, J M; Small, K W; Jones, M A et al. (1990) Confirmation of linkage in von Hippel-Lindau disease. Genomics 6:565-7

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