Biology:International System for Human Cytogenetic Nomenclature
From HandWiki
The International System for Human Cytogenetic Nomenclature (note: since 2016 edition name was changed to International System for Human CYTOGENOMIC Nomenclature) (ISCN) is an international standard for human chromosome nomenclature, which includes band names, symbols and abbreviated terms used in the description of human chromosome and chromosome abnormalities. The ISCN used as the central reference among cytogeneticists since 1960.[1][2]
Revision history
- ISCN (2020). S. Karger Publishing. ISBN:978-3318068672
- ISCN (2016). S. Karger Publishing. ISBN:978-3318058574
- ISCN (2013). S. Karger Publishing. ISBN:978-3318022537
- ISCN (2009). S. Karger Publishing. ISBN:978-3805589857
- ISCN (2005). S. Karger Publishing. ISBN:978-3805580199
- ISCN (1995). S. Karger Publishing. ISBN:978-3805562263
- ISCN (1991). S. Karger Publishing. ISBN:978-3805555678
- ISCN (1985). S. Karger Publishing. ISBN:978-3805538701
- ISCN (1981). S. Karger Publishing. ISBN:978-3805534840
- ISCN (1978). S. Karger Publishing. ISBN:978-3805530118
- Paris Conference (1971): "Standardization in Human Cytogenetics." (PDF) Birth Defects: Original Article Series, Vol 8, No 7 (The National Foundation, New York 1972)
- Chicago Conference (1966): "Standardization in Human Cytogenetics." Birth Defects: Original Article Series, Vol 2, No 2 (The National Foundation, New York 1966).
- London Conference (1963): "London Conference on the Normal Human Karyotype." Cytogenetics 2:264–268 (1963)
- Denver Conference (1960): "A proposed standard system of nomenclature of human mitotic chromosomes." The Lancet 275.7133 (1960): 1063-1065.
See also
References
- ↑ Slovak M.L., Theisen A., Shaffer L.G. (2013) "Human Chromosome Nomenclature: An Overview and Definition of Terms." In: Gersen S., Keagle M. (eds) The Principles of Clinical Cytogenetics. Springer, New York, NY doi:10.1007/978-1-4419-1688-4_3
- ↑ "Nomenclature evolution: Changes in the ISCN from the 2005 to the 2009 edition.". Cytogenet Genome Res 127 (1): 1–4. 2009. doi:10.1159/000279442. PMID 20110655.
External links
- About the ISCN recommendations - Human Genome Variation Society
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