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181 results

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Page 1
Genotype-phenotype correlations in MYCN-related Feingold syndrome.
Marcelis CL, Hol FA, Graham GE, Rieu PN, Kellermayer R, Meijer RP, Lugtenberg D, Scheffer H, van Bokhoven H, Brunner HG, de Brouwer AP. Marcelis CL, et al. Among authors: kellermayer r. Hum Mutat. 2008 Sep;29(9):1125-32. doi: 10.1002/humu.20750. Hum Mutat. 2008. PMID: 18470948
Expanding the clinical spectrum of MYCN-related Feingold syndrome.
Tészás A, Meijer R, Scheffer H, Gyuris P, Kosztolányi G, van Bokhoven H, Kellermayer R. Tészás A, et al. Among authors: kellermayer r. Am J Med Genet A. 2006 Oct 15;140(20):2254-6. doi: 10.1002/ajmg.a.31407. Am J Med Genet A. 2006. PMID: 16906565 No abstract available.
Vertebral defects in a patient with Feingold syndrome.
Kellermayer R, Weisenbach J, Gyuris P, Aszmann M, Kosztolányi G. Kellermayer R, et al. Clin Dysmorphol. 2005 Oct;14(4):213-214. Clin Dysmorphol. 2005. PMID: 16155427 No abstract available.
Lithium suppresses epidermal SERCA2 and PMR1 levels in the rat.
Süle N, Tészás A, Kálmán E, Szigeti R, Miseta A, Kellermayer R. Süle N, et al. Among authors: kellermayer r. Pathol Oncol Res. 2006;12(4):234-6. doi: 10.1007/BF02893419. Epub 2006 Dec 25. Pathol Oncol Res. 2006. PMID: 17189987 Free article.
Upper gastrointestinal malformations in Coffin-Siris syndrome.
Kellermayer R, Kitagawa S, Redel CA, Cass DL, Belmont JW, Klish W. Kellermayer R, et al. Am J Med Genet A. 2007 Jul 1;143A(13):1519-21. doi: 10.1002/ajmg.a.31865. Am J Med Genet A. 2007. PMID: 17523151 Review. No abstract available.
Alpha-thalassemia/mental retardation syndrome in a 45,X male.
Kellermayer R, Czakó M, Kiss-László Z, Gyuris P, Kozári A, Melegh B, Kosztolányi G. Kellermayer R, et al. Am J Med Genet A. 2005 Feb 1;132A(4):431-3. doi: 10.1002/ajmg.a.30499. Am J Med Genet A. 2005. PMID: 15633163 Review.
181 results