[kroh-muh-proh-teen, -tee-in] /ˌkroʊ məˈproʊ tin, -ti ɪn/
a , as hemoglobin or rhodopsin, containing a pigmented nonprotein group, such as heme, riboflavin, or retinal.
any of a group of conjugated proteins, such as haemoglobin, in which the protein is joined to a coloured compound, such as a metal-containing porphyrin
noun, Genetics. 1. any irregularity or abnormality of chromosome distribution, number, structure, or arrangement.
- Chromosomal instability syndrome
chromosomal instability syndrome n. Any of a group of Mendelian inheritance conditions associated with chromosomal instability and breakage in vitro and often leading to an increased tendency to develop certain types of malignancies. Also called chromosomal breakage syndrome.
- Chromosomal map
chromosomal map n. A representation of the karyotype and of the positioning and ordering on it of those loci that have been localized by any of several mapping methods.
- Chromosomal region
chromosomal region n. The part of a chromosome defined either by anatomical details, especially by banding, or by its linkage groups.