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Homozygous condition for a BrdU-requiring fragile site on chromosome 12
I Voiculescu1, E Back, W Schempp
1Institut für Humangenetik und Anthropologie der Universität, Freiburg, Federal Republic of Germany.
Human Genetics
|February 1, 1991
Abstract:
A rare BrdU-sensitive fragile site, designated FRA12C*RQ24.2 has a relatively high frequency in the normal population. It can be demonstrated in a heterozygous and homozygous condition. There is no evidence that a phenotypic abnormality is associated with the expression of this site. A comparison with the fragile site FRA10B*RQ25.2 has revealed common features with FRA12C*RQ24.2.