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ISCN

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16號染色體的圖示

國際人類細胞遺傳命名系統(英語:International System for Human Cytogenetic Nomenclature,縮寫ISCN)是一個人類染色體命名法的國際標準,它規定了人類染色體的多個方面包括帶名稱、染色體異常等術語及縮寫,如q表示染色體長臂,p表示染色體短臂等。自初版在1960年發佈以來對細胞遺傳學的發展起到了重要作用。[1][2]

版本歷史

  • 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)頁面存檔備份,存於互聯網檔案館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.

參考文獻

  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可免費查閱.