No evidence for a paternal interchromosomal effect from analysis of the origin of nondisjunction in Down syndrome patients with concomitant familial chromosome rearrangements.

Lignende værker

• Nondisjunction of chromosome 15: origin and recombination.
  af: Robinson, W P, et al.
  Udgivet: (1993)
• Multiple origins of X chromosome tetrasomy.
  af: Robinson, W P, et al.
  Udgivet: (1994)
• Analysis of DNA polymorphisms suggests that most de novo dup(21q) chromosomes in patients with Down syndrome are isochromosomes and not translocations.
  af: Antonarakis, S E, et al.
  Udgivet: (1990)
• Down syndrome due to de novo Robertsonian translocation t(14q;21q): DNA polymorphism analysis suggests that the origin of the extra 21q is maternal.
  af: Petersen, M B, et al.
  Udgivet: (1991)
• Investigation of Factors Associated With Paternal Nondisjunction of Chromosome 21
  af: Oliver, Tiffany Renee, et al.
  Udgivet: (2009)