Congenital anomalies due to transmission of a chromosome translocation.

Ítems similars

• A family showing transmission of a translocation between a 6-12 chromosome and a 21-22 chromosome.
  per: Gray, J E, et al.
  Publicat: (1966)
• Multiple congenital anomalies associated with a ring-D chromosome.
  per: Juberg, R C, et al.
  Publicat: (1969)
• Pyloric atresia. A hereditary congenital anomaly with autosomal recessive transmission.
  per: Bar-Maor, J A, et al.
  Publicat: (1972)
• An interstitial deletion of chromosome 9 in a girl with multiple congenital anomalies.
  per: Wisniewski, L, et al.
  Publicat: (1977)
• Chromosomal translocation in a family with ocular anomalies: indications for karyotype analysis
  per: Jamieson, R V, et al.
  Publicat: (2003)