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Screening for Tay-Sachs disease carriers by full-exon sequencing with novel variant interpretation outperforms enzyme testing in a pan-ethnic cohort.
Cecchi AC, Vengoechea ES, Kaseniit KE, Hardy MW, Kiger LA, Mehta N, Haque IS, Moyer K, Page PZ, Muzzey D, Grinzaid KA. Cecchi AC, et al. Among authors: hardy mw. Mol Genet Genomic Med. 2019 Aug;7(8):e836. doi: 10.1002/mgg3.836. Epub 2019 Jul 10. Mol Genet Genomic Med. 2019. PMID: 31293106 Free PMC article.
Telehealth for genetic counseling: A systematic evidence review.
Danylchuk NR, Cook L, Shane-Carson KP, Cacioppo CN, Hardy MW, Nusbaum R, Steelman SC, Malinowski J. Danylchuk NR, et al. Among authors: hardy mw. J Genet Couns. 2021 Oct;30(5):1361-1378. doi: 10.1002/jgc4.1481. Epub 2021 Aug 6. J Genet Couns. 2021. PMID: 34355839
AUTOMATED INSTRUCTION FOR RETARDED CHILDREN.
MALPASS LF, HARDY MW, GILMORE AS, WILLIAMS CF. MALPASS LF, et al. Among authors: hardy mw. Am J Ment Defic. 1964 Nov;69:405-12. Am J Ment Defic. 1964. PMID: 14223558 No abstract available.
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