Clinical Findings Associated with a De Novo Partial Trisomy 10p11.22p15.3 and Monosomy 7p22.3 Detected by Chromosomal Microarray Analysis

Podobne zapisy

• Clinical Findings Associated with a De Novo Partial Trisomy 10p11.22p15.3 and Monosomy 7p22.3 Detected by Chromosomal Microarray Analysis
  od: Kohannim, Omid, i wsp.
  Wydane: (2011)
• Two cases of partial trisomy 8p and partial monosomy 21q in a family with a reciprocal translocation (8;21)(p21.1;q22.3).
  od: Plomp, A S, i wsp.
  Wydane: (1998)
• Three children with partial trisomy 1q and partial monosomy 3p.
  od: McCarthy, G T, i wsp.
  Wydane: (1986)
• Partial Trisomy 3p and Monosomy 7p Associated with Tetralogy of Fallot and Infantile Seizure
  od: Chia-Ming Chang, i wsp.
  Wydane: (2007-09-01)
• Familial t(8;15)(p23.3;q22.3): report of two cases with dup(15) (q22.3----qter).
  od: Goldstein, D J, i wsp.
  Wydane: (1987)