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Page 1
National Society of Genetic Counselors Code of Ethics: Explication of 2017 Revisions.
Senter L, Bennett RL, Madeo AC, Noblin S, Ormond KE, Schneider KW, Swan K, Virani A; National Society of Genetic Counselors Code of Ethics Review Task Force (COERTF). Senter L, et al. Among authors: madeo ac. J Genet Couns. 2018 Feb;27(1):9-15. doi: 10.1007/s10897-017-0165-9. Epub 2017 Oct 27. J Genet Couns. 2018. PMID: 29075947
Use of SLC26A4 mutation testing for unilateral enlargement of the vestibular aqueduct.
Chattaraj P, Reimold FR, Muskett JA, Shmukler BE, Chien WW, Madeo AC, Pryor SP, Zalewski CK, Butman JA, Brewer CC, Kenna MA, Alper SL, Griffith AJ. Chattaraj P, et al. Among authors: madeo ac. JAMA Otolaryngol Head Neck Surg. 2013 Sep;139(9):907-13. doi: 10.1001/jamaoto.2013.4185. JAMA Otolaryngol Head Neck Surg. 2013. PMID: 24051746
A mutation of PCDH15 among Ashkenazi Jews with the type 1 Usher syndrome.
Ben-Yosef T, Ness SL, Madeo AC, Bar-Lev A, Wolfman JH, Ahmed ZM, Desnick RJ, Willner JP, Avraham KB, Ostrer H, Oddoux C, Griffith AJ, Friedman TB. Ben-Yosef T, et al. Among authors: madeo ac. N Engl J Med. 2003 Apr 24;348(17):1664-70. doi: 10.1056/NEJMoa021502. N Engl J Med. 2003. PMID: 12711741 Free article. No abstract available.
Allelic hierarchy of CDH23 mutations causing non-syndromic deafness DFNB12 or Usher syndrome USH1D in compound heterozygotes.
Schultz JM, Bhatti R, Madeo AC, Turriff A, Muskett JA, Zalewski CK, King KA, Ahmed ZM, Riazuddin S, Ahmad N, Hussain Z, Qasim M, Kahn SN, Meltzer MR, Liu XZ, Munisamy M, Ghosh M, Rehm HL, Tsilou ET, Griffith AJ, Zein WM, Brewer CC, Riazuddin S, Friedman TB. Schultz JM, et al. Among authors: madeo ac. J Med Genet. 2011 Nov;48(11):767-75. doi: 10.1136/jmedgenet-2011-100262. Epub 2011 Sep 22. J Med Genet. 2011. PMID: 21940737
22 results