Alport Syndrome - Genetics of X-Linked and Autosomal Form

Agency: National Institute of Health (NIH)
Institute: National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type: Research Project (R01)
Project #: 5R01DK043761-05
Application #: 2143263
Study Section: General Medicine B Study Section (GMB)


NIH 1998 R01 DK	Alport Syndrome - Genetics of X-Linked and Autosomal Form Barker, David F. / University of Utah
NIH 1997 R01 DK	Alport Syndrome - Genetics of X-Linked and Autosomal Form Barker, David F. / University of Utah
NIH 1996 R01 DK	Alport Syndrome - Genetics of X-Linked and Autosomal Form Barker, David F. / University of Utah
NIH 1995 R01 DK	Alport Syndrome - Genetics of X-Linked and Autosomal Form Barker, David F. / University of Utah
NIH 1994 R01 DK	Alport Syndrome Genetics and Mutation Detection Barker, David F. / University of Utah
NIH 1993 R01 DK	Alport Syndrome Genetics and Mutation Detection Barker, David F. / University of Utah
NIH 1992 R01 DK	Alport Syndrome Genetics and Mutation Detection Barker, David F. / University of Utah

Barker, D F; Denison, J C; Atkin, C L et al. (2001) Efficient detection of Alport syndrome COL4A5 mutations with multiplex genomic PCR-SSCP. Am J Med Genet 98:148-60

Barker, D F; Denison, J C; Atkin, C L et al. (1997) Common ancestry of three Ashkenazi-American families with Alport syndrome and COL4A5 R1677Q. Hum Genet 99:681-4

Fain, P R; Kort, E N; Chance, P F et al. (1995) A 2D crossover-based map of the human X chromosome as a model for map integration. Nat Genet 9:261-6

Barker, D F; Cordray, P; Fain, P R (1994) The same polymorphism identified by the DXS571(B) and DXS1105 loci. Hum Mol Genet 3:1913