Functional deficiency of fibroblasts heterozygous for Bloom syndrome as specific manifestation of the primary defect.

Ítems similars

• Rate of sister chromatid exchanges in Bloom syndrome fibroblasts reduced by co-cultivation with normal fibroblasts.
  per: Rüdiger, H W, et al.
  Publicat: (1980)
• Clastogenic activity from Bloom syndrome fibroblast cultures.
  per: Emerit, I, et al.
  Publicat: (1981)
• Elevated spontaneous mutation rate in Bloom syndrome fibroblasts.
  per: Warren, S T, et al.
  Publicat: (1981)
• Cellular defects caused by hypomorphic variants of the Bloom syndrome helicase gene BLM
  per: Shastri, Vivek M., et al.
  Publicat: (2015)
• The hyperimmunoglobulin E syndrome - clinical manifestation diversity in primary immune deficiency
  per: Szczawinska-Poplonyk Aleksandra, et al.
  Publicat: (2011-11-01)