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

Ítems similars

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