• MeSH
• chromozomy MeSH
• cytogenetika MeSH
• terminologie jako téma MeSH
• Publikační typ
• monografie MeSH

• Konspekt
• Biologické vědy
• NLK Obory
• genetika, lékařská genetika
• biologie

This publication combines and extends the now classic system of human cytogenetic nomenclature prepared by expert committees and published in collaboration with Cytogenetic and Genome Research (formerly: Cytogenetics and Cell Genetics) since 1963. Revised and finalized by the ISCN Committee and its advisors at a meeting in Vancouver, BC, in December 2004, it updates, corrects and incorporates all previous human cytogenetic nomenclature recommendations into one systematically organized publication. It thus supersedes the previous compilations in \"ISCN 1985\" and its supplement, \"ISCN 1991\", the Guidelines for Cancer Cytogenetics, and \"ISCN 1995\". What\'s new in \"ISCN 2005\"? The G- and R-banded karyotypes have been replaced by new ones reflecting higher band-level resolutions. New ideograms at the 300-band and 700-band level have been added. The in situ hybridization nomenclature has been modernized, simplified, and expanded. New examples reflecting unique situations are included. A basic nomenclature for recording array comparative genomic hybridization results is introduced. \"ISCN 2005\" also contains a detachable fold-out of the normal human karyotype, consisting of photographs of G-banded and R-banded chromosomes at the commonly examined 550-band resolution stage and their diagrammatic representations - a useful aid for human cytogeneticists, technicians, and students.

International system for human cytogenetic nomenclature (2009)

Doporučení Stálého mezinárodního výboru

Publikováno ve spolupráci s Cytogenetic and Genome Research

Obsahuje bibliografii a rejstřík

Normal chromosomes -- Symbols and abbreviated terms -- Karyotype designation -- Uncertainty in chromosome or band designation -- Order of chromosome abnormalities in the karyotype -- Normal variable chromosome features -- Numerical chromosome abnormalities -- Structural chromosome rearrangements -- Chromosome breakage -- Neoplasia -- Meiotic chromosomes -- In situ hybridization -- Copy number detection.