Founder effect at PGL1 in hereditary head and neck paraganglioma families from the Netherlands.

Ítems similars

• First experiences with genetic counselling based on predictive DNA diagnosis in hereditary glomus tumours (paragangliomas).
  per: Oosterwijk, J C, et al.
  Publicat: (1996)
• Similar gene expression profiles of sporadic, PGL2-, and SDHD-linked paragangliomas suggest a common pathway to tumorigenesis
  per: Hensen, Erik F, et al.
  Publicat: (2009)
• DNA flow cytometry of hereditary and sporadic paragangliomas (glomus tumours).
  per: van der Mey, A. G., et al.
  Publicat: (1991)
• The Clinical Phenotype of SDHC-Associated Hereditary Paraganglioma Syndrome (PGL3)
  per: Else, Tobias, et al.
  Publicat: (2014)
• The Dutch founder mutation SDHD.D92Y shows a reduced penetrance for the development of paragangliomas in a large multigenerational family
  per: Hensen, Erik F, et al.
  Publicat: (2010)