A new case of familial paracentric inversion of chromosome 2
- PMID: 3817813
- DOI: 10.1007/BF00591087
A new case of familial paracentric inversion of chromosome 2
Abstract
A phenotypically otherwise normal homosexual man with a 46,XY,inv(2)(q21q33) karyotype inherited from his mother is described. The breakpoints were different from those observed in the only other case of familial paracentric inversion of chromosome 2 reported in the literature, but in our case they seem to correspond to constitutive and aphidicolin-induced fragile sites.