Arnos KS - Search Results

1

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: arnos ks. Hum Hered. 1995 Sep-Oct;45(5):243-52. doi: 10.1159/000154307. Hum Hered. 1995. PMID: 7590754

2

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: arnos ks. Am J Med Genet. 1995 Jul 17;57(4):540-7. doi: 10.1002/ajmg.1320570405. Am J Med Genet. 1995. PMID: 7573125

3

Major-locus contributions to variability of the craniofacial feature dystopia canthorum in Waardenburg syndrome.

Reynolds JE, Marazita ML, Meyer JM, Stevens CA, Eaves LJ, Arnos KS, Ploughman LM, MacLean C, Nance WE, Diehl SR. Reynolds JE, et al. Among authors: arnos ks. Am J Hum Genet. 1996 Feb;58(2):384-92. Am J Hum Genet. 1996. PMID: 8571965 Free PMC article.

4

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: arnos ks. Hum Mol Genet. 1996 Apr;5(4):497-502. doi: 10.1093/hmg/5.4.497. Hum Mol Genet. 1996. PMID: 8845842

5

Ascertainment of families with hereditary deafness for linkage studies. Waardenburg and Usher syndromes.

Stevens C, Arnos K, Bodurtha J, Wright L, Rawlings B, Marazita M, Nance W, Diehl S. Stevens C, et al. Ann N Y Acad Sci. 1991;630:293-4. doi: 10.1111/j.1749-6632.1991.tb19610.x. Ann N Y Acad Sci. 1991. PMID: 1952611 No abstract available.

6

Genetic epidemiological studies of early-onset deafness in the U.S. school-age population.

Marazita ML, Ploughman LM, Rawlings B, Remington E, Arnos KS, Nance WE. Marazita ML, et al. Among authors: arnos ks. Am J Med Genet. 1993 Jun 15;46(5):486-91. doi: 10.1002/ajmg.1320460504. Am J Med Genet. 1993. PMID: 8322805

7

Further comments on the genetics of prelingual deafness.

Marazita ML, Nance WE, Arnos KS. Marazita ML, et al. Among authors: arnos ks. Am J Hum Genet. 1989 Oct;45(4):637-8. Am J Hum Genet. 1989. PMID: 2491020 Free PMC article. No abstract available.

8

Innovative approach to genetic counseling services for the deaf population.

Arnos KS, Cunningham M, Israel J, Marazita ML. Arnos KS, et al. Am J Med Genet. 1992 Oct 1;44(3):345-51. doi: 10.1002/ajmg.1320440315. Am J Med Genet. 1992. PMID: 1488983

9

Locus heterogeneity for Waardenburg syndrome is predictive of clinical subtypes.

Farrer LA, Arnos KS, Asher JH Jr, Baldwin CT, Diehl SR, Friedman TB, Greenberg J, Grundfast KM, Hoth C, Lalwani AK, et al. Farrer LA, et al. Among authors: arnos ks. Am J Hum Genet. 1994 Oct;55(4):728-37. Am J Hum Genet. 1994. PMID: 7942851 Free PMC article.

10

Correlation between Waardenburg syndrome phenotype and genotype in a population of individuals with identified PAX3 mutations.

DeStefano AL, Cupples LA, Arnos KS, Asher JH Jr, Baldwin CT, Blanton S, Carey ML, da Silva EO, Friedman TB, Greenberg J, Lalwani AK, Milunsky A, Nance WE, Pandya A, Ramesar RS, Read AP, Tassabejhi M, Wilcox ER, Farrer LA. DeStefano AL, et al. Among authors: arnos ks. Hum Genet. 1998 May;102(5):499-506. doi: 10.1007/s004390050732. Hum Genet. 1998. PMID: 9654197

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