Agency
National Institute of Health (NIH)
Institute
National Human Genome Research Institute (NHGRI)
Type
Research Project (R01)
Project #
5R01HG000457-06
Application #
2208846
Study Section
Genome Study Section (GNM)
Project Start
1991-09-30
Project End
1998-06-30
Budget Start
1996-07-01
Budget End
1998-06-30
Support Year
6
Fiscal Year
1996
Total Cost
Indirect Cost
Name
University of Iowa
Department
Pediatrics
Type
Schools of Medicine
DUNS #
041294109
City
Iowa City
State
IA
Country
United States
Zip Code
52242
Green, Glenn E; Scott, Daryl A; McDonald, Joshua M et al. (2002) Performance of cochlear implant recipients with GJB2-related deafness. Am J Med Genet 109:167-70
Campbell, C; Cucci, R A; Prasad, S et al. (2001) Pendred syndrome, DFNB4, and PDS/SLC26A4 identification of eight novel mutations and possible genotype-phenotype correlations. Hum Mutat 17:403-11
Scott, D A; Drury, S; Sundstrom, R A et al. (2000) Refining the DFNB7-DFNB11 deafness locus using intragenic polymorphisms in a novel gene, TMEM2. Gene 246:265-74
Green, G E; Scott, D A; McDonald, J M et al. (1999) Carrier rates in the midwestern United States for GJB2 mutations causing inherited deafness. JAMA 281:2211-6
Scott, D A; Wang, R; Kreman, T M et al. (1999) The Pendred syndrome gene encodes a chloride-iodide transport protein. Nat Genet 21:440-3
Scott, D A; Greinwald Jr, J H; Marietta, J R et al. (1998) Identification and mutation analysis of a cochlear-expressed, zinc finger protein gene at the DFNB7/11 and dn hearing-loss loci on human chromosome 9q and mouse chromosome 19. Gene 215:461-9
Brennan, T M; Landau, D; Shalev, H et al. (1998) Linkage of infantile Bartter syndrome with sensorineural deafness to chromosome 1p. Am J Hum Genet 62:355-61
Parvari, R; Hershkovitz, E; Kanis, A et al. (1998) Homozygosity and linkage-disequilibrium mapping of the syndrome of congenital hypoparathyroidism, growth and mental retardation, and dysmorphism to a 1-cM interval on chromosome 1q42-43. Am J Hum Genet 63:163-9
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
Heaney, C; Shalev, H; Elbedour, K et al. (1998) Human autosomal recessive osteopetrosis maps to 11q13, a position predicted by comparative mapping of the murine osteosclerosis (oc) mutation. Hum Mol Genet 7:1407-10

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