http://www.loc.gov/mods/v3 http://www.loc.gov/standards/mods/v3/mods-3-2.xsd
an international system for human cytogenomic nomenclature (2016)
International system for human cytogenomic nomenclature (2016)
International Standing Committee on Human Cytogenomic Nomenclature
Historical introduction -- 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 -- Miicroarrays -- Region-speciifc assays -- Sequence-based assays.
editors, Jean McGowan-Jordan, Ottawa, Ont., Annet Simons, Nijmegen, Michael Schmid, Würzburg.
"Recommendations of the International Standing Committee on Human Cytogenomic Nomenclature, including new sequence-based cytogenomic nomenclature developed in collaboration with the Human Genome Variation Society (HGVS) Sequence Variant Description Working Group."
Publicado en Cytogenetic and Genome Research vol. 149, no. 1-2 (2016) bajo el título ISCN 2016: An International System for Human Cytogenomic Nomenclature.
Incluye referencias bibliográficas e índice analítico.