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

Ítems similars

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