Splotch locus mouse mutants: models for neural tube defects and Waardenburg syndrome type I in humans.

Samankaltaisia teoksia

• Assignment of the locus for Waardenburg syndrome type I to human chromosome 2q37 and possible homology to the Splotch mouse.
  Tekijä: Foy, C, et al.
  Julkaistu: (1990)
• Mouse and hamster mutants as models for Waardenburg syndromes in humans.
  Tekijä: Asher, J H, et al.
  Julkaistu: (1990)
• Meckel syndrome and neural tube defects in Kuwait.
  Tekijä: Teebi, A S, et al.
  Julkaistu: (1992)
• Prevention of Neural Tube Defects in Lrp Mutant Mouse Embryos by Folic Acid Supplementation
  Tekijä: Sabatino, Julia A., et al.
  Julkaistu: (2017)
• Molecular basis of splotch and Waardenburg Pax-3 mutations.
  Tekijä: Chalepakis, G, et al.
  Julkaistu: (1994)