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Allelic heterogeneity of alkaptonuria in Central Europe.
Müller CR, Fregin A, Srsen S, Srsnova K, Halliger-Keller B, Felbor U, Seemanova E, Kress W. Müller CR, et al. Among authors: srsnova k. Eur J Hum Genet. 1999 Sep;7(6):645-51. doi: 10.1038/sj.ejhg.5200343. Eur J Hum Genet. 1999. PMID: 10482952
Molecular defects in alkaptonuria.
Gehrig A, Schmidt SR, Müller CR, Srsen S, Srsnova K, Kress W. Gehrig A, et al. Among authors: srsnova k. Cytogenet Cell Genet. 1997;76(1-2):14-6. doi: 10.1159/000134501. Cytogenet Cell Genet. 1997. PMID: 9154114
The human gene for alkaptonuria (AKU) maps to chromosome 3q.
Janocha S, Wolz W, Srsen S, Srsnova K, Montagutelli X, Guénet JL, Grimm T, Kress W, Müller CR. Janocha S, et al. Among authors: srsnova k. Genomics. 1994 Jan 1;19(1):5-8. doi: 10.1006/geno.1994.1003. Genomics. 1994. PMID: 8188241
Diagnosis of alkaptonuria in children.
Srsen S, Srsnová K. Srsen S, et al. Among authors: srsnova k. Padiatr Padol. 1979;14(2):163-7. Padiatr Padol. 1979. PMID: 460920
[Alkaptonuria and the HLA system (author's transl)].
Srsen S, Nyulassy S, Buc M, Srsnová K. Srsen S, et al. Among authors: srsnova k. Cas Lek Cesk. 1978 Dec 8;117(49):1523-5. Cas Lek Cesk. 1978. PMID: 576112 Slovak. No abstract available.
35 results