Dominant piebald trait in a retarded child with a reciprocal translocation and small intercalary deletion.

Samankaltaisia teoksia

• Piebald trait in a retarded child with interstitial deletion of chromosome 4.
  Tekijä: Lacassie, Y, et al.
  Julkaistu: (1977)
• Concurrence of dominant piebald trait and fragile X syndrome.
  Tekijä: Finucane, B, et al.
  Julkaistu: (1991)
• Two reciprocal translocations associated with microcephaly and retardation.
  Tekijä: Bell, E F, et al.
  Julkaistu: (1977)
• Dominant piebald trait (white forelock and leukoderma) with neurological impairment.
  Tekijä: Telfer, M A, et al.
  Julkaistu: (1971)
• Deletion of the c-kit protooncogene in the human developmental defect piebald trait.
  Tekijä: Fleischman, R A, et al.
  Julkaistu: (1991)