国际人类细胞遗传命名系统（英语：International System for Human Cytogenetic Nomenclature，缩写ISCN）是一个人类染色体命名法的国际标准，它规定了人类染色体的多个方面包括带名称、染色体异常等术语及缩写，如q表示染色体长臂，p表示染色体短臂等。自初版在1960年发布以来对细胞遗传学的发展起到了重要作用。[1][2]
版本历史
- 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) （页面存档备份，存于互联网档案馆） 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.
参考文献
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