ISCN :  an international system for human cytogenomic nomenclature (2016) / 
 International system for human cytogenomic nomenclature (2016) 
editors, Jean McGowan-Jordan, Ottawa, Ont., Annet Simons, Nijmegen, Michael Schmid, Würzburg. 
 - vi, 139 p. :  il. ;  28 cm. 
<br/><br/> "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. 
<br/><br/>Incluye referencias bibliográficas e índice analítico. 
<br/><br/>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. 
<br/><br/><label>ISBN: </label>9783318058574 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Cytogenetics--Terminology.<br/>Genomics--Terminology.<br/>CROMOSOMAS<br/>CARIOTIPO<br/>ABERRACIONES CROMOSOMICAS<br/>HIBRIDACION IN-SITU<br/>CROMOSOMAS EN ANILLO<br/>CLASIFICACION CROMOSOMICA<br/>TERMINOLOGIA NORMALIZADA
<br/><br/><label>Universal Decimal Class. No.: </label>575.1 (083.72)