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Intrafamilial variability of limb-girdle muscular dystrophy, LGMD1D type.
Zima J, Eaton A, Pál E, Till Á, Ito YA, Warman-Chardon J, Hartley T, Cagnone G, Melegh BI; Care4Rare Canada; Boycott KM, Melegh B, Hadzsiev K. Zima J, et al. Among authors: melegh b, melegh bi. Eur J Med Genet. 2020 Feb;63(2):103655. doi: 10.1016/j.ejmg.2019.04.012. Epub 2019 Apr 27. Eur J Med Genet. 2020. PMID: 31034989
Refining the South Asian Origin of the Romani people.
Melegh BI, Banfai Z, Hadzsiev K, Miseta A, Melegh B. Melegh BI, et al. Among authors: melegh b. BMC Genet. 2017 Aug 31;18(1):82. doi: 10.1186/s12863-017-0547-x. BMC Genet. 2017. PMID: 28859608 Free PMC article.
Erratum to: Non-syndromic Hearing Impairment in a Hungarian Family with the m.7510T>C Mutation of Mitochondrial tRNA(Ser(UCN)) and Review of Published Cases.
Komlósi K, Maász A, Kisfali P, Hadzsiev K, Bene J, Melegh BI, Ablonczy M, Németh K, Fekete G, Melegh B. Komlósi K, et al. Among authors: melegh b, melegh bi. JIMD Rep. 2013;9:E1. doi: 10.1007/978-3-642-35518-9_195. Epub 2012 Nov 2. JIMD Rep. 2013. PMID: 23832234 Free PMC article. No abstract available.
Hearing impairment locus heterogeneity and identification of PLS1 as a new autosomal dominant gene in Hungarian Roma.
Schrauwen I, Melegh BI, Chakchouk I, Acharya A, Nasir A, Poston A, Cornejo-Sanchez DM, Szabo Z, Karosi T, Bene J, Melegh B, Leal SM. Schrauwen I, et al. Among authors: melegh b, melegh bi. Eur J Hum Genet. 2019 Jun;27(6):869-878. doi: 10.1038/s41431-019-0372-y. Epub 2019 Mar 14. Eur J Hum Genet. 2019. PMID: 30872814 Free PMC article. Clinical Trial.
Interethnic variability of CYP4F2 (V433M) in admixed population of Roma and Hungarians.
Sipeky C, Weber A, Melegh BI, Matyas P, Janicsek I, Szalai R, Szabo I, Varnai R, Tarlos G, Ganczer A, Melegh B. Sipeky C, et al. Among authors: melegh b, melegh bi. Environ Toxicol Pharmacol. 2015 Jul;40(1):280-3. doi: 10.1016/j.etap.2015.05.008. Epub 2015 May 22. Environ Toxicol Pharmacol. 2015. PMID: 26176903
438 results