Koopiaarvu variatsioonid (Estonian Wikipedia)

Analysis of information sources in references of the Wikipedia article "Koopiaarvu variatsioonid" in Estonian language version.

refsWebsite

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nih.gov

Genetics Home Reference, "Copy number variation", published October 2014, http://ghr.nlm.nih.gov/glossary=copynumbervariation; kasutatud 12.10.2014 (inglise)
Genetics Home Reference, "Chromosome 21", reviewed November 2013, http://ghr.nlm.nih.gov/chromosome/21; kasutatud 03.10.2014 (inglise)
Genetics Home Reference, "Turner syndrome", reviewed January 2012, http://ghr.nlm.nih.gov/condition/turner-syndrome; kasutatud 03.10.2014 (inglise)
Genetics Home Reference, "Klinefelter syndrome", reviewed January 2013, http://ghr.nlm.nih.gov/condition/klinefelter-syndrome; kasutatud 03.10.2014 (inglise)
Genetics Home Reference, "Li-Fraumeni syndrome", reviewed January 2007, http://ghr.nlm.nih.gov/condition/li-fraumeni-syndrome; kasutatud 03.10.2014 (inglise)

Charles Lee and Stephen W. Schere (2010) The clinical context of copy number variation in the human genome. Expert Rev. Mol. Med. Vol.12, e8, March 2010. http://www.ncbi.nlm.nih.gov/pubmed/20211047, kasutatud 12.10.2014 (inglise)
Feng Zhang, Mehrdad Khajavi, Anne M Connolly, Charles F Towne, Sat Dev Batish & James R Lupski. The DNA replication FoSTeS/MMBIR mechanism can generate genomic, genic and exonic complex rearrangements in humans. Nature Genetics, volume 41, number 7, July 2009. http://www.ncbi.nlm.nih.gov/pubmed/19543269, kasutatud 12.10.2014 (inglise)

MedlinePlus, "Cri du chat syndrome", 08.09.2013, http://www.nlm.nih.gov/medlineplus/ency/article/001593.htm; kasutatud 03.10.2014 (inglise)

Charlotte N. Henrichsen, Evelyne Chaignat and Alexandre Reymond. Copy number variants, diseases and gene expression. Human Molecular Genetics, 2009, Vol. 18, Review Issue 1 R1–R8. http://hmg.oxfordjournals.org/content/18/R1/R1.full; kasutatud 08.10.2014 (inglise)

Database of Genomic Variants, "About the project", http://dgv.tcag.ca/dgv/app/about?ref=NCBI36/hg18; kasutatud 03.10.2014 (inglise)

Wenli Li and Michael Olivier. Current analysis platforms and methods for detecting copy number variation. Physiol Genomics 45: 1–16, 2013. https://web.archive.org/web/20130905113245/http://physiolgenomics.physiology.org/content/45/1/1.short; kasutatud 08.10.14 (inglise)
Asper Biotech, "Geneetika põhimõisted", https://web.archive.org/web/20151118002230/http://www.asper.ee/fakte-geneetikast/geneetika-pohimoisted/, kasutatud 05.10.14
Projektid, "EuroEPINOMICS – Genetics of rare epilepsy syndromes (RES)", June 2011 – May 2014, https://web.archive.org/web/20141017041643/http://www.geenivaramu.ee/et/projektid; kasutatud 11.10.2014 (inglise)
Biotehnoloogia, Inimese molekulaargeneetika õppegrupp, https://web.archive.org/web/20141019162214/http://www.tymri.ut.ee/et/instituudist/biotehnoloogia; kasutatud 11.10.2014

Choy K, Setlur S, Lee C, Lau T. The impact of human copy number variation on a new era of genetic testing. BJOG 2010;117:391–398. http://onlinelibrary.wiley.com/doi/10.1111/j.1471-0528.2009.02470.x/full; kasutatud 08.10.14 (inglise)