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[Molecular genetic diagnosis of neurofibromatosis type I].
Polgár N, Komlósi K, Hadzsiev K, Illés T, Melegh B. Polgár N, et al. Among authors: hadzsiev k. Orv Hetil. 2011 Mar 13;152(11):415-9. doi: 10.1556/OH.2011.29059. Orv Hetil. 2011. PMID: 21362601 Hungarian.
Mitochondrial dysfunction and organic aciduria in five patients carrying mutations in the Ras-MAPK pathway.
Kleefstra T, Wortmann SB, Rodenburg RJ, Bongers EM, Hadzsiev K, Noordam C, van den Heuvel LP, Nillesen WM, Hollody K, Gillessen-Kaesbach G, Lammens M, Smeitink JA, van der Burgt I, Morava E. Kleefstra T, et al. Among authors: hadzsiev k. Eur J Hum Genet. 2011 Feb;19(2):138-44. doi: 10.1038/ejhg.2010.171. Epub 2010 Nov 10. Eur J Hum Genet. 2011. PMID: 21063443 Free PMC article.
A unique haplotype of RCCX copy number variation: from the clinics of congenital adrenal hyperplasia to evolutionary genetics.
Doleschall M, Luczay A, Koncz K, Hadzsiev K, Erhardt É, Szilágyi Á, Doleschall Z, Németh K, Török D, Prohászka Z, Gereben B, Fekete G, Gláz E, Igaz P, Korbonits M, Tóth M, Rácz K, Patócs A. Doleschall M, et al. Among authors: hadzsiev k. Eur J Hum Genet. 2017 Jun;25(6):702-710. doi: 10.1038/ejhg.2017.38. Epub 2017 Apr 12. Eur J Hum Genet. 2017. PMID: 28401898 Free PMC article.
Rehabilitation needs of a genetic counseling unit.
Aszmann M, Hadzsiev K, Kosztolányi G. Aszmann M, et al. Among authors: hadzsiev k. Genet Couns. 2005;16(4):417-9. Genet Couns. 2005. PMID: 16440886 No abstract available.
94 results