Landa B - Search Results

1

A novel locus for autosomal dominant non-syndromic deafness (DFNA41) maps to chromosome 12q24-qter.

Blanton SH, Liang CY, Cai MW, Pandya A, Du LL, Landa B, Mummalanni S, Li KS, Chen ZY, Qin XN, Liu YF, Balkany T, Nance WE, Liu XZ. Blanton SH, et al. Among authors: landa b. J Med Genet. 2002 Aug;39(8):567-70. doi: 10.1136/jmg.39.8.567. J Med Genet. 2002. PMID: 12161595 Free PMC article.

2

Haplotype analysis of the USH1D locus and genotype-phenotype correlations.

Liu XZ, Blanton SH, Bitner-Glindzicz M, Pandya A, Landa B, MacArdle B, Rajput K, Bellman S, Webb BT, Ping X, Smith RJ, Nance WE. Liu XZ, et al. Among authors: landa b. Clin Genet. 2001 Jul;60(1):58-62. doi: 10.1034/j.1399-0004.2001.600109.x. Clin Genet. 2001. PMID: 11531971

3

Phenotypic variation in Waardenburg syndrome: mutational heterogeneity, modifier genes or polygenic background?

Pandya A, Xia XJ, Landa BL, Arnos KS, Israel J, Lloyd J, James AL, Diehl SR, Blanton SH, Nance WE. Pandya A, et al. Among authors: landa bl. Hum Mol Genet. 1996 Apr;5(4):497-502. doi: 10.1093/hmg/5.4.497. Hum Mol Genet. 1996. PMID: 8845842

4

Fine mapping of the human biotinidase gene and haplotype analysis of five common mutations.

Blanton SH, Pandya A, Landa BL, Javaheri R, Xia X, Nance WE, Pomponio RJ, Norrgard KJ, Swango KL, Demirkol M, Gülden H, Coskun T, Tokatli A, Ozalp I, Wolf B. Blanton SH, et al. Among authors: landa bl. Hum Hered. 2000 Mar-Apr;50(2):102-11. doi: 10.1159/000022897. Hum Hered. 2000. PMID: 10799968

5

Linkage studies in a large kindred with hereditary pancreatitis confirms mapping of the gene to a 16-cM region on 7q.

Pandya A, Blanton SH, Landa B, Javaheri R, Melvin E, Nance WE, Markello T. Pandya A, et al. Among authors: landa b. Genomics. 1996 Dec 1;38(2):227-30. doi: 10.1006/geno.1996.0620. Genomics. 1996. PMID: 8954806

6

Implications of molecular diagnostic testing in families with hereditary pancreatitis.

Pandya A, Xia XJ, Blanton SH, Landa B, Markello T, Nance WE. Pandya A, et al. Among authors: landa b. Genet Test. 1997-1998;1(3):207-11. doi: 10.1089/gte.1997.1.207. Genet Test. 1997. PMID: 10464647

7

Analysis of variability of clinical manifestations in Waardenburg syndrome.

Reynolds JE, Meyer JM, Landa B, Stevens CA, Arnos KS, Israel J, Marazita ML, Bodurtha J, Nance WE, Diehl SR. Reynolds JE, et al. Among authors: landa b. Am J Med Genet. 1995 Jul 17;57(4):540-7. doi: 10.1002/ajmg.1320570405. Am J Med Genet. 1995. PMID: 7573125

8

Prenatal diagnosis of heterozygosity for biotinidase deficiency by enzymatic and molecular analyses.

Pomponio RJ, Hymes J, Pandya A, Landa B, Melone P, Javaheri R, Mardach R, Morton SW, Meyers GA, Reynolds T, Buck G, Nance WE, Wolf B. Pomponio RJ, et al. Among authors: landa b. Prenat Diagn. 1998 Feb;18(2):117-22. Prenat Diagn. 1998. PMID: 9516011

9

Heterogenous point mutations in the mitochondrial tRNA Ser(UCN) precursor coexisting with the A1555G mutation in deaf students from Mongolia.

Pandya A, Xia XJ, Erdenetungalag R, Amendola M, Landa B, Radnaabazar J, Dangaasuren B, Van Tuyle G, Nance WE. Pandya A, et al. Among authors: landa b. Am J Hum Genet. 1999 Dec;65(6):1803-6. doi: 10.1086/302658. Am J Hum Genet. 1999. PMID: 10577941 Free PMC article. No abstract available.

10

Analysis of locus heterogeneity in Waardenburg syndrome types 1 and 2 using highly informative microsatellite markers.

Reynolds JE, Arnos KS, Landa B, Stevens CA, Salbert BA, Wright L, Duke B, Hunt W, Marazita ML, Ploughman L, et al. Reynolds JE, et al. Among authors: landa b. Hum Hered. 1995 Sep-Oct;45(5):243-52. doi: 10.1159/000154307. Hum Hered. 1995. PMID: 7590754

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