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Analysis of short tandem repeat (STR) allele frequency distributions in a Balinese population.
Hum Mol Genet. 1995 Jan;4(1):85-91. doi: 10.1093/hmg/4.1.85.
Hum Mol Genet. 1995.
PMID: 7711738
Congenital non-syndromal autosomal recessive deafness in Bengkala, an isolated Balinese village.
Winata S, Arhya IN, Moeljopawiro S, Hinnant JT, Liang Y, Friedman TB, Asher JH Jr.
Winata S, et al. Among authors: hinnant jt.
J Med Genet. 1995 May;32(5):336-43. doi: 10.1136/jmg.32.5.336.
J Med Genet. 1995.
PMID: 7616538
Free PMC article.
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A gene for congenital, recessive deafness DFNB3 maps to the pericentromeric region of chromosome 17.
Friedman TB, Liang Y, Weber JL, Hinnant JT, Barber TD, Winata S, Arhya IN, Asher JH Jr.
Friedman TB, et al. Among authors: hinnant jt.
Nat Genet. 1995 Jan;9(1):86-91. doi: 10.1038/ng0195-86.
Nat Genet. 1995.
PMID: 7704031
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Genetic mapping refines DFNB3 to 17p11.2, suggests multiple alleles of DFNB3, and supports homology to the mouse model shaker-2.
Liang Y, Wang A, Probst FJ, Arhya IN, Barber TD, Chen KS, Deshmukh D, Dolan DF, Hinnant JT, Carter LE, Jain PK, Lalwani AK, Li XC, Lupski JR, Moeljopawiro S, Morell R, Negrini C, Wilcox ER, Winata S, Camper SA, Friedman TB.
Liang Y, et al. Among authors: hinnant jt.
Am J Hum Genet. 1998 Apr;62(4):904-15. doi: 10.1086/301786.
Am J Hum Genet. 1998.
PMID: 9529344
Free PMC article.
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Challenges and solutions for gene identification in the presence of familial locus heterogeneity.
Rehman AU, Santos-Cortez RL, Drummond MC, Shahzad M, Lee K, Morell RJ, Ansar M, Jan A, Wang X, Aziz A, Riazuddin S, Smith JD, Wang GT, Ahmed ZM, Gul K, Shearer AE, Smith RJ, Shendure J, Bamshad MJ, Nickerson DA; University of Washington Center for Mendelian Genomics; Hinnant J, Khan SN, Fisher RA, Ahmad W, Friderici KH, Riazuddin S, Friedman TB, Wilch ES, Leal SM.
Rehman AU, et al.
Eur J Hum Genet. 2015 Sep;23(9):1207-15. doi: 10.1038/ejhg.2014.266. Epub 2014 Dec 10.
Eur J Hum Genet. 2015.
PMID: 25491636
Free PMC article.
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DFNB3 families and Shaker-2 mice: mutations in an unconventional myosin, myo 15.
Friedman TB, Hinnant JT, Fridell RA, Wilcox ER, Raphael Y, Camper SA.
Friedman TB, et al. Among authors: hinnant jt.
Adv Otorhinolaryngol. 2000;56:131-44. doi: 10.1159/000059094.
Adv Otorhinolaryngol. 2000.
PMID: 10868225
Review.
No abstract available.
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DFNB3, spectrum of MYO15A recessive mutant alleles and an emerging genotype-phenotype correlation.
Friedman TB, Hinnant JT, Ghosh M, Boger ET, Riazuddin S, Lupski JR, Potocki L, Wilcox ER.
Friedman TB, et al. Among authors: hinnant jt.
Adv Otorhinolaryngol. 2002;61:124-30. doi: 10.1159/000066824.
Adv Otorhinolaryngol. 2002.
PMID: 12408074
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