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Mouse models and genetic modifiers in X-linked adrenoleukodystrophy.
Heinzer AK, McGuinness MC, Lu JF, Stine OC, Wei H, Van der Vlies M, Dong GX, Powers J, Watkins PA, Smith KD. Heinzer AK, et al. Among authors: stine oc. Adv Exp Med Biol. 2003;544:75-93. doi: 10.1007/978-1-4419-9072-3_12. Adv Exp Med Biol. 2003. PMID: 14713218 Review. No abstract available.
Adrenoleukodystrophy: phenotypic variability and implications for therapy.
Moser HW, Moser AB, Smith KD, Bergin A, Borel J, Shankroff J, Stine OC, Merette C, Ott J, Krivit W, et al. Moser HW, et al. Among authors: stine oc. J Inherit Metab Dis. 1992;15(4):645-64. doi: 10.1007/BF01799621. J Inherit Metab Dis. 1992. PMID: 1528023 Review.
Phenotypic characterization of individuals with 30-40 CAG repeats in the Huntington disease (HD) gene reveals HD cases with 36 repeats and apparently normal elderly individuals with 36-39 repeats.
Rubinsztein DC, Leggo J, Coles R, Almqvist E, Biancalana V, Cassiman JJ, Chotai K, Connarty M, Crauford D, Curtis A, Curtis D, Davidson MJ, Differ AM, Dode C, Dodge A, Frontali M, Ranen NG, Stine OC, Sherr M, Abbott MH, Franz ML, Graham CA, Harper PS, Hedreen JC, Hayden MR, et al. Rubinsztein DC, et al. Among authors: stine oc. Am J Hum Genet. 1996 Jul;59(1):16-22. Am J Hum Genet. 1996. PMID: 8659522 Free PMC article.
217 results