Transmission of a t(13q22q) chromosome observed in three generations with segregation of the translocation D1-trisomy syndrome

@article{Abe1975TransmissionOA,
  title={Transmission of a t(13q22q) chromosome observed in three generations with segregation of the translocation D1-trisomy syndrome},
  author={Tatsuo Abe and Masuji Morita and Kenji Kawai and Shinichi Misawa and Hideo Kanai and Genjiro Hirose and Hiroko Fujita},
  journal={Humangenetik},
  year={1975},
  volume={30},
  pages={207-215}
}
A case of an inherited type of D/G translocation D1-trisomy syndrome was described. A female proposita who had the clinical signs of D1-trisomy syndrome was found to have a chromosome complement of 46,XX,-G,+t(DqGq). Examination of Q- and G-stained karyotypes revealed that the chromosomes involved in the translocation were members of Nos. 13 and 22, or t(13q22q) with breaks at p12 of both chromosomes. C-stained figures also showed a large heterochromatin block in its centromeric region. The t… CONTINUE READING
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