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Geographical and ethnic variation of the 677C>T allele of 5,10 methylenetetrahydrofolate reductase (MTHFR): findings from over 7000 newborns from 16 areas world wide.
Wilcken B, Bamforth F, Li Z, Zhu H, Ritvanen A, Renlund M, Stoll C, Alembik Y, Dott B, Czeizel AE, Gelman-Kohan Z, Scarano G, Bianca S, Ettore G, Tenconi R, Bellato S, Scala I, Mutchinick OM, López MA, de Walle H, Hofstra R, Joutchenko L, Kavteladze L, Bermejo E, Martínez-Frías ML, Gallagher M, Erickson JD, Vollset SE, Mastroiacovo P, Andria G, Botto LD. Wilcken B, et al. Among authors: lopez ma. J Med Genet. 2003 Aug;40(8):619-25. doi: 10.1136/jmg.40.8.619. J Med Genet. 2003. PMID: 12920077 Free PMC article. No abstract available.
Clinical phenotype associated with terminal 2q37 deletion.
Conrad B, Dewald G, Christensen E, Lopez M, Higgins J, Pierpont ME. Conrad B, et al. Clin Genet. 1995 Sep;48(3):134-9. doi: 10.1111/j.1399-0004.1995.tb04073.x. Clin Genet. 1995. PMID: 8556820 Review.
Implementing Entrustable Professional Activities in Pediatric Fellowships: Facilitating the Process.
Langhan ML, Boyer DL, Hsu D, Moffatt ME, Pitts SA, Atlas MP, Aye T, Chess P, Curran ML, Czaja AS, Dammann CEL, Fussell J, George RP, Herman BE, High P, James SH, Kamin DS, Karnik R, Kesselheim J, Lopez MA, Mahan JD, McFadden V, McGann KA, Mehta JJ, Rama J, Robinson BW, Sauer C, Stafford DEJ, Turner DA, Weiss P, Yussman SM, Schwartz A, Mink R. Langhan ML, et al. Among authors: lopez ma. Pediatrics. 2024 May 17:e2023065024. doi: 10.1542/peds.2023-065024. Online ahead of print. Pediatrics. 2024. PMID: 38757175
624 results