Combined association of Presenilin-1 and Apolipoprotein E polymorphisms with maternal meiosis II error in Down syndrome births

Gelijkaardige items

• An intronic rare mutation in Presenilin-1 (PSEN-1) gene may be involved in the developement of Alzheimer’s disease
  door: Bhaumik, Pranami, et al.
  Gepubliceerd in: (2014)
• COL6A1 loss of function mutation underlie atrioventricular septal defects in down syndrome patients
  door: Ghosh, Priyanka, et al.
  Gepubliceerd in: (2014)
• Altered incidence of meiotic errors and Down syndrome birth under extreme low socioeconomic exposure in the Sundarban area of India
  door: Ghosh, Sujoy, et al.
  Gepubliceerd in: (2013)
• Etiology of Down Syndrome: Evidence for Consistent Association among Altered Meiotic Recombination, Nondisjunction and Maternal Age Across Populations
  door: Ghosh, Sujoy, et al.
  Gepubliceerd in: (2009)
• The etiology of Down syndrome: Maternal MCM9 polymorphisms increase risk of reduced recombination and nondisjunction of chromosome 21 during meiosis I within oocyte
  door: Pal, Upamanyu, et al.
  Gepubliceerd in: (2021)