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ISCN

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16号染色体的图示

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

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  • 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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  1. ^ 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
  2. ^ Brothman AR, Persons DL, Shaffer LG. Nomenclature evolution: Changes in the ISCN from the 2005 to the 2009 edition.. Cytogenet Genome Res. 2009, 127 (1): 1–4. PMID 20110655. doi:10.1159/000279442可免费查阅.