Publication | Open Access
Manitoba Aboriginal Kindred with Original Cerebro-Oculo-Facio-Skeletal Syndrome Has a Mutation in the Cockayne Syndrome Group B (CSB) Gene
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Citations
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References
2000
Year
Mendelian DisorderGenetic DisorderManitoba Aboriginal KindredGeneticsGenetic EpidemiologyPathologyMolecular GeneticsGenetic VariationGenomicsMedicine
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