Extra small marker chromosome associated with normal phenotype due to 3:1 disjunction of t(14;22) in a parent. Implications for the origin of marker chromosomes
Karen Bröndum-NielsenVolume:
40
Year:
1991
Language:
english
Pages:
3
DOI:
10.1111/j.1399-0004.1991.tb03079.x
File:
PDF, 152 KB
english, 1991