This database consists of a systematic collection of citations from the world's literature reporting on all common and rare chromosomal alterations, phenotypes, and abnormalities in humans. The database is organized by variations and anomalies, numerical anomalies, and chromosomal breakage syndromes. It contains over 24,000 entries updated continuously since 1974. The database documents information on the availability of mutant cell lines and presents chromosome alterations with a list that cross-references band numbers. For human and medical geneticists, cytogeneticists, cytogenetic laboratory technicians, and others interested in human chromosome abnormalities. Developed by Digamber S. Borgaonkar, PhD.
Related titles: Also called: Chromosomal Variation in Man : a Catalog of Chromosomal Variants and Anomalies