Common genetic variation contributes significantly to the risk of childhood B-cell precursor acute lymphoblastic leukemia

Míreanna comhchosúla

• Common genetic variation contributes significantly to the risk of childhood B-cell precursor acute lymphoblastic leukemia.
  de réir: Enciso-Mora, V, et al.
  Foilsithe / Cruthaithe: (2012)
• Genome-wide homozygosity signatures and childhood acute lymphoblastic leukemia risk.
  de réir: Hosking, F, et al.
  Foilsithe / Cruthaithe: (2010)
• MHC variation and risk of childhood B-cell precursor acute lymphoblastic leukemia.
  de réir: Hosking, F, et al.
  Foilsithe / Cruthaithe: (2011)
• Loci on 7p12.2, 10q21.2 and 14q11.2 are associated with risk of childhood acute lymphoblastic leukemia.
  de réir: Papaemmanuil, E, et al.
  Foilsithe / Cruthaithe: (2009)
• Variation in CDKN2A at 9p21.3 influences childhood acute lymphoblastic leukemia risk.
  de réir: Sherborne, A, et al.
  Foilsithe / Cruthaithe: (2010)