Down's syndrome associated with two Robertsonian translocations, 45,XX,−15,−21,+t(15q21q) and 46,XX,−21,+t(21q21q)

Samankaltaisia teoksia

• Mosaic Down's syndrome with de novo 45,XX,-21,-22,+t(21q;22q)/46,XX,-21,+t(21q;21q) rearrangement.
  Tekijä: Tharapel, A T, et al.
  Julkaistu: (1984)
• Karyotype 45,XX,−21/46,XX,21q− in an infant with symptoms of G-deletion syndrome I
  Tekijä: Mikkelsen, Margareta, et al.
  Julkaistu: (1974)
• Monozygotic twins discordant for homologous Robertsonian translocation trisomy 21 of 46, XX, + 21, der (21;21) (q10; q10) in a twin-to-twin transfusion syndrome, case report
  Tekijä: Cao, Dingya, et al.
  Julkaistu: (2021)
• Balanced Robertsonian translocation mosaicism of mosaic 45,XY,der(13;21) (q10;q10)/46,XY at amniocentesis in a pregnancy with a favorable outcome and no perinatal decrease of the cell line with the balanced Robertsonian translocation
  Tekijä: Chih-Ping Chen
  Julkaistu: (2024-07-01)
• Down syndrome due to de novo Robertsonian translocation t(14q;21q): DNA polymorphism analysis suggests that the origin of the extra 21q is maternal.
  Tekijä: Petersen, M B, et al.
  Julkaistu: (1991)