Pelias MZ - Search Results

1

Localization of two genes for Usher syndrome type I to chromosome 11.

Smith RJ, Lee EC, Kimberling WJ, Daiger SP, Pelias MZ, Keats BJ, Jay M, Bird A, Reardon W, Guest M, et al. Smith RJ, et al. Among authors: pelias mz. Genomics. 1992 Dec;14(4):995-1002. doi: 10.1016/s0888-7543(05)80122-3. Genomics. 1992. PMID: 1478678

2

Clinical variability and genetic heterogeneity within the Acadian Usher population.

Smith RJ, Pelias MZ, Daiger SP, Keats B, Kimberling W, Hejtmancik JF. Smith RJ, et al. Among authors: pelias mz. Am J Med Genet. 1992 Aug 1;43(6):964-9. doi: 10.1002/ajmg.1320430612. Am J Med Genet. 1992. PMID: 1415347

3

Linkage studies of Usher syndrome type 1: exclusion results from the Usher syndrome consortium.

Keats BJ, Todorov AA, Atwood LD, Pelias MZ, Hejtmancik JF, Kimberling WJ, Leppert M, Lewis RA, Smith RJ. Keats BJ, et al. Among authors: pelias mz. Genomics. 1992 Nov;14(3):707-14. doi: 10.1016/s0888-7543(05)80172-7. Genomics. 1992. PMID: 1427898

4

Clinical diagnosis of the Usher syndromes. Usher Syndrome Consortium.

Smith RJ, Berlin CI, Hejtmancik JF, Keats BJ, Kimberling WJ, Lewis RA, Möller CG, Pelias MZ, Tranebjaerg L. Smith RJ, et al. Among authors: pelias mz. Am J Med Genet. 1994 Mar 1;50(1):32-8. doi: 10.1002/ajmg.1320500107. Am J Med Genet. 1994. PMID: 8160750

5

Exclusion of Usher syndrome gene from much of chromosome 4.

Smith RJ, Holcomb JD, Daiger SP, Caskey CT, Pelias MZ, Alford BR, Fontenot DD, Hejtmancik JF. Smith RJ, et al. Among authors: pelias mz. Cytogenet Cell Genet. 1989;50(2-3):102-6. doi: 10.1159/000132733. Cytogenet Cell Genet. 1989. PMID: 2776474

6

Tightly linked flanking microsatellite markers for the Usher syndrome type I locus on the short arm of chromosome 11.

Keats BJ, Nouri N, Pelias MZ, Deininger PL, Litt M. Keats BJ, et al. Among authors: pelias mz. Am J Hum Genet. 1994 Apr;54(4):681-6. Am J Hum Genet. 1994. PMID: 8128966 Free PMC article.

7

Fine mapping of the usher syndrome type IC to chromosome 11p14 and identification of flanking markers by haplotype analysis.

Ayyagari R, Li Y, Smith RJ, Pelias MZ, Hejtmancik JF. Ayyagari R, et al. Among authors: pelias mz. Mol Vis. 1995 Oct 25;1:2. Mol Vis. 1995. PMID: 9238080 Free article.

8

Assembly of a high-resolution map of the Acadian Usher syndrome region and localization of the nuclear EF-hand acidic gene.

DeAngelis MM, Doucet JP, Drury S, Sherry ST, Robichaux MB, Den Z, Pelias MZ, Ditta GM, Keats BJ, Deininger PL, Batzer MA. DeAngelis MM, et al. Among authors: pelias mz. Biochim Biophys Acta. 1998 Jul 1;1407(1):84-91. doi: 10.1016/s0925-4439(98)00025-8. Biochim Biophys Acta. 1998. PMID: 9639681 Free article.

9

DNA linkage studies of degenerative retinal diseases.

Daiger SP, Heckenlively JR, Lewis RA, Pelias MZ. Daiger SP, et al. Among authors: pelias mz. Prog Clin Biol Res. 1987;247:147-62. Prog Clin Biol Res. 1987. PMID: 3317443 Review.

10

Linkage studies of Usher syndrome: analysis of an Acadian kindred in Louisiana.

Pelias MZ, Lemoine DR, Kossar AL, Ward LJ, Wilson AF, Elston RC. Pelias MZ, et al. Cytogenet Cell Genet. 1988;47(1-2):111-2. doi: 10.1159/000132524. Cytogenet Cell Genet. 1988. PMID: 3162715 No abstract available.

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