Uniparental disomy 7 in Silver-Russell syndrome and primordial growth retardation
Kotzot, D, Schmitt, S, Bernasconi, F, Robinson, W P, Lurie, I W, Ilyina, H, Méhes, K, Hamel, B C, Otten, B J, Hergersberg, M
Published in Human molecular genetics (01.04.1995)
Published in Human molecular genetics (01.04.1995)
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Increased prevalence of factor V Leiden mutation in neonatal intracranial haemorrhage
Melegh, B, Stankovics, J, Kis, A, Nagy, A, Storcz, J, Losonczy, H, Méhes, K
Published in European journal of pediatrics (01.03.1998)
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Published in European journal of pediatrics (01.03.1998)
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Umbilical venous catheterization and development of Banti syndrome: the possible role of the factor V Leiden mutation
Stankovics, J, Nagy, A, Méhes, K, Melegh, B
Published in European journal of pediatrics (01.08.1998)
Published in European journal of pediatrics (01.08.1998)
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Constitutional aneuploidy and cancer predisposition caused by biallelic mutations in BUB1B
Méhes, Károly, Shannon, Nora, FitzPatrick, David, Reid, Sarah, Douglas, Jenny, Firth, Helen, Plaja, Alberto, Robin, Nathanial, Irrthum, Alexandre, Nash, Richard, Tolmie, John, Kidd, Alexa, Swansbury, John, Coleman, Kim, Hanks, Sandra, Rahman, Nazneen
Published in Nature genetics (01.11.2004)
Published in Nature genetics (01.11.2004)
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Plasma carnitine ester profile in homozygous and heterozygous OCTN2 deficiency
Komlósi, K., Magyari, L., Talián, G. C., Nemes, É., Káposzta, R., Mogyorósy, G., Méhes, K., Melegh, B.
Published in Journal of inherited metabolic disease (01.12.2009)
Published in Journal of inherited metabolic disease (01.12.2009)
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No latent chromosome damage in oxygen-exposed premature neonates
Méhes, K, Bajnóczky, K, Adamovich, K, Khezri, S, Kosztolányi, G
Published in Journal of human genetics (01.01.1999)
Published in Journal of human genetics (01.01.1999)
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Multiple mitochondrial DNA deletions and persistent hyperthermia in a patient with Brachmann-de Lange phenotype
Melegh, B, Bock, I, Gáti, I, Méhes, K
Published in American journal of medical genetics (02.10.1996)
Published in American journal of medical genetics (02.10.1996)
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Increased frequency of the C3F allele and the Leiden mutation of coagulation factor V in patients with severe coronary heart disease who survived myocardial infarction
Császár, A, Duba, J, Melegh, B, Kramer, J, Szalai, C, Prohászka, Z, Karádi, I, Kovács, M, Méhes, K, Romics, L, Füst, G
Published in Experimental and clinical immunogenetics (01.01.2001)
Published in Experimental and clinical immunogenetics (01.01.2001)
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