Meiotic consequences of pericentric inversions of chromosome 13
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference34 articles.
1. Transmission of a t(13q22q) chromosome observed in three generations with segregation of the translocation D1-trisomy syndrome
2. Localization of heterochromatin in human chromosomes
3. (ed): “Birth Defects Compendium,” ed 2. New York: Alan R. Liss, Inc, National Foundation March of Dimes, 1977, pp 212-213.
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