Agency
National Institute of Health (NIH)
Institute
National Human Genome Research Institute (NHGRI)
Type
Specialized Center (P50)
Project #
1P50HG000835-01
Application #
3843229
Study Section
Project Start
Project End
Budget Start
Budget End
Support Year
1
Fiscal Year
1992
Total Cost
Indirect Cost
Name
University of Iowa
Department
Type
DUNS #
041294109
City
Iowa City
State
IA
Country
United States
Zip Code
52242
Taillon-Miller, P; Bauer-Sardina, I; Saccone, N L et al. (2000) Juxtaposed regions of extensive and minimal linkage disequilibrium in human Xq25 and Xq28. Nat Genet 25:324-8
Gleeson, C M; Sloan, J M; McGuigan, J A et al. (1998) Barrett's oesophagus: microsatellite analysis provides evidence to support the proposed metaplasia-dysplasia-carcinoma sequence. Genes Chromosomes Cancer 21:49-60
Scott, D A; Kraft, M L; Carmi, R et al. (1998) Identification of mutations in the connexin 26 gene that cause autosomal recessive nonsyndromic hearing loss. Hum Mutat 11:387-94
el-Shanti, H; Murray, J C; Semina, E V et al. (1998) Assignment of gene responsible for progressive pseudorheumatoid dysplasia to chromosome 6 and examination of COL10A1 as candidate gene. Eur J Hum Genet 6:251-6
Greinwald Jr, J H; Scott, D A; Marietta, J R et al. (1997) Construction of P1-derived artificial chromosome and yeast artificial chromosome contigs encompassing the DFNB7 and DFNB11 region of chromosome 9q13-21. Genome Res 7:879-86
Yuan, B; Vaske, D; Weber, J L et al. (1997) Improved set of short-tandem-repeat polymorphisms for screening the human genome. Am J Hum Genet 60:459-60
Sheffield, V C; Pierpont, M E; Nishimura, D et al. (1997) Identification of a complex congenital heart defect susceptibility locus by using DNA pooling and shared segment analysis. Hum Mol Genet 6:117-21
Peiffer-Schneider, S; Schutte, B C; Murray, J C et al. (1997) Exclusion of Ifa and Ifb as the Lps gene and mapping of three markers near the Lps locus. Mamm Genome 8:785-6
Gleeson, C M; Sloan, J M; McGuigan, J A et al. (1997) Allelotype analysis of adenocarcinoma of the gastric cardia. Br J Cancer 76:1455-65
Bonne-Tamir, B; Nystuen, A; Seroussi, E et al. (1997) Usher syndrome in the Samaritans: strengths and limitations of using inbred isolated populations to identify genes causing recessive disorders. Am J Phys Anthropol 104:193-200

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