Jednonukleotidový polymorfismus (Czech Wikipedia)

Analysis of information sources in references of the Wikipedia article "Jednonukleotidový polymorfismus" in Czech language version.

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ZHANG, Kui; QIN, Zhaohui S.; LIU, Jun S.; CHEN, Ting; WATERMAN, Michael S.; SUN, Fengzhu. Haplotype Block Partitioning and Tag SNP Selection Using Genotype Data and Their Applications to Association Studies. S. 908–916. Genome Research [online]. 2004-05. Roč. 14, čís. 5, s. 908–916. Dostupné online. DOI 10.1101/gr.1837404. (anglicky)

INGRAM, V. M. A specific chemical difference between the globins of normal human and sickle-cell anaemia haemoglobin. Nature. 13 October 1956, s. 792–794. DOI 10.1038/178792a0. PMID 13369537.
CHANG, J. C.; KAN, Y. W. Beta 0 thalassemia, a nonsense mutation in man. Proceedings of the National Academy of Sciences of the United States of America. June 1979, s. 2886–2889. DOI 10.1073/pnas.76.6.2886. PMID 88735.
WOLF, A. B.; CASELLI, R. J.; REIMAN, E. M.; VALLA, J. APOE and neuroenergetics: An emerging paradigm in Alzheimer's disease. Neurobiology of Aging. April 2013, s. 1007–17. DOI 10.1016/j.neurobiolaging.2012.10.011. PMID 23159550.
ZHANG, Kui; QIN, Zhaohui S.; LIU, Jun S.; CHEN, Ting; WATERMAN, Michael S.; SUN, Fengzhu. Haplotype Block Partitioning and Tag SNP Selection Using Genotype Data and Their Applications to Association Studies. S. 908–916. Genome Research [online]. 2004-05. Roč. 14, čís. 5, s. 908–916. Dostupné online. DOI 10.1101/gr.1837404. (anglicky)
Nachman, Michael W. Single-nucleotide polymorphisms and recombination rate in humans. Trends in Genetics. September 2001, s. 481–485. DOI 10.1016/S0168-9525(01)02409-X. PMID 11525814.
M. A. Varela; W. AMOS. Heterogeneous distribution of SNPs in the human genome: Microsatellites as predictors of nucleotide diversity and divergence. Genomics. March 2010, s. 151–159. DOI 10.1016/j.ygeno.2009.12.003. PMID 20026267.

single-nucleotide polymorphism / SNP | Learn Science at Scitable [online]. [cit. 2015-11-13]. Dostupné online.

INGRAM, V. M. A specific chemical difference between the globins of normal human and sickle-cell anaemia haemoglobin. Nature. 13 October 1956, s. 792–794. DOI 10.1038/178792a0. PMID 13369537.
CHANG, J. C.; KAN, Y. W. Beta 0 thalassemia, a nonsense mutation in man. Proceedings of the National Academy of Sciences of the United States of America. June 1979, s. 2886–2889. DOI 10.1073/pnas.76.6.2886. PMID 88735.
HAMOSH, A.; KING, T. M.; ROSENSTEIN, B. J.; COREY, M.; LEVISON, H.; DURIE, P.; TSUI, L. C. Cystic fibrosis patients bearing both the common missense mutation Gly----Asp at codon 551 and the delta F508 mutation are clinically indistinguishable from delta F508 homozygotes, except for decreased risk of meconium ileus. American Journal of Human Genetics. August 1992, s. 245–250. PMID 1379413.
WOLF, A. B.; CASELLI, R. J.; REIMAN, E. M.; VALLA, J. APOE and neuroenergetics: An emerging paradigm in Alzheimer's disease. Neurobiology of Aging. April 2013, s. 1007–17. DOI 10.1016/j.neurobiolaging.2012.10.011. PMID 23159550.
Nachman, Michael W. Single-nucleotide polymorphisms and recombination rate in humans. Trends in Genetics. September 2001, s. 481–485. DOI 10.1016/S0168-9525(01)02409-X. PMID 11525814.
M. A. Varela; W. AMOS. Heterogeneous distribution of SNPs in the human genome: Microsatellites as predictors of nucleotide diversity and divergence. Genomics. March 2010, s. 151–159. DOI 10.1016/j.ygeno.2009.12.003. PMID 20026267.