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181 results

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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.
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.
Congenital chylothorax in Opitz G/BBB syndrome.
Funke S, Kellermayer R, Czakó M, So J, Kosztolányi G, Ertl T. Funke S, et al. Among authors: kellermayer r. Am J Med Genet A. 2006 May 15;140(10):1119-21. doi: 10.1002/ajmg.a.31224. Am J Med Genet A. 2006. PMID: 16619207 No abstract available.
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
A cryptic unbalanced translocation resulting in del 13q and dup 15q.
Tészás A, Møller RS, Kellermayer R, Czakó M, Kjaer KW, Ullmann R, Melegh B, Tommerup N, Kosztolányi G. Tészás A, et al. Among authors: kellermayer r. Am J Med Genet A. 2008 Oct 1;146A(19):2570-3. doi: 10.1002/ajmg.a.32394. Am J Med Genet A. 2008. PMID: 18792978 No abstract available.
181 results