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11 results

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Page 1
Audiometric tests of speech defective college students.
HEGARTY IE, MILLER VR. HEGARTY IE, et al. Among authors: miller vr. J Speech Disord. 1948 Dec;13(4):361-5. doi: 10.1044/jshd.1304.361. J Speech Disord. 1948. PMID: 18105500 No abstract available.
ClinGen's GenomeConnect registry enables patient-centered data sharing.
Savatt JM, Azzariti DR, Faucett WA, Harrison S, Hart J, Kattman B, Landrum MJ, Ledbetter DH, Miller VR, Palen E, Rehm HL, Rhode J, Turner S, Vidal JA, Wain KE, Riggs ER, Martin CL. Savatt JM, et al. Among authors: miller vr. Hum Mutat. 2018 Nov;39(11):1668-1676. doi: 10.1002/humu.23633. Hum Mutat. 2018. PMID: 30311371 Free PMC article.
The RD-Connect Registry & Biobank Finder: a tool for sharing aggregated data and metadata among rare disease researchers.
Gainotti S, Torreri P, Wang CM, Reihs R, Mueller H, Heslop E, Roos M, Badowska DM, de Paulis F, Kodra Y, Carta C, Martìn EL, Miller VR, Filocamo M, Mora M, Thompson M, Rubinstein Y, Posada de la Paz M, Monaco L, Lochmüller H, Taruscio D. Gainotti S, et al. Among authors: miller vr. Eur J Hum Genet. 2018 May;26(5):631-643. doi: 10.1038/s41431-017-0085-z. Epub 2018 Feb 2. Eur J Hum Genet. 2018. PMID: 29396563 Free PMC article.
Response to Horn et al.
de Souza MP, Miller VR. de Souza MP, et al. Among authors: miller vr. J Invest Dermatol. 2013 May;133(5):1362. doi: 10.1038/jid.2012.470. Epub 2013 Jan 17. J Invest Dermatol. 2013. PMID: 23325015 Free article. No abstract available.
Informed consent process for patient participation in rare disease registries linked to biorepositories.
Rubinstein YR, Groft SC, Chandros SH, Kaneshiro J, Karp B, Lockhart NC, Marshall PA, Moxley RT 3rd, Pollen GB, Miller VR, Schwartz J. Rubinstein YR, et al. Among authors: miller vr. Contemp Clin Trials. 2012 Jan;33(1):5-11. doi: 10.1016/j.cct.2011.10.004. Epub 2011 Oct 24. Contemp Clin Trials. 2012. PMID: 22036955 Free PMC article. Review. No abstract available.
Quality assurance for Duchenne and Becker muscular dystrophy genetic testing: development of a genomic DNA reference material panel.
Kalman L, Leonard J, Gerry N, Tarleton J, Bridges C, Gastier-Foster JM, Pyatt RE, Stonerock E, Johnson MA, Richards CS, Schrijver I, Ma T, Miller VR, Adadevoh Y, Furlong P, Beiswanger C, Toji L. Kalman L, et al. Among authors: miller vr. J Mol Diagn. 2011 Mar;13(2):167-74. doi: 10.1016/j.jmoldx.2010.11.018. J Mol Diagn. 2011. PMID: 21354051 Free PMC article.
Creating a global rare disease patient registry linked to a rare diseases biorepository database: Rare Disease-HUB (RD-HUB).
Rubinstein YR, Groft SC, Bartek R, Brown K, Christensen RA, Collier E, Farber A, Farmer J, Ferguson JH, Forrest CB, Lockhart NC, McCurdy KR, Moore H, Pollen GB, Richesson R, Miller VR, Hull S, Vaught J. Rubinstein YR, et al. Among authors: miller vr. Contemp Clin Trials. 2010 Sep;31(5):394-404. doi: 10.1016/j.cct.2010.06.007. Epub 2010 Jul 8. Contemp Clin Trials. 2010. PMID: 20609392 Free PMC article.
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