Cytogenetischer Befund und Ätiologie bei Fanconi-Anämie

@article{Schroder2004CytogenetischerBU,
  title={Cytogenetischer Befund und {\"A}tiologie bei Fanconi-An{\"a}mie},
  author={Traute M. Schroder},
  journal={Humangenetik},
  year={2004},
  volume={3},
  pages={76-81}
}
In addition to findings in four cases of Fanconi's anemia with hexokinase deficiency recently reported we are able to show cytogenetic results in a further case without any defect in carbohydrate metabolism. Cultures were made from peripheral blood. 30% of the mitoses showed chromatid type aberrations. Although the findings in this case no. 274 proved to be similar to those of the other patients, there are some differences, however. In this case 1. the number of chromatid breaks is smaller, 2… CONTINUE READING