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Weyers acrofacial dysostosis

Curry-Hall syndrome
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Research Articles from PubMed

Research articles describe the outcome of a single study. They are the published results of original research. The terms "Weyers acrofacial dysostosis" returned 0 free, full-text research articles. First 0 results:
A novel heterozygous deletion in the EVC2 gene causes Weyers acrofacial dysostosis.
Last Updated: Nov 13, 2018

Weyers acrofacial dysostosis (MIM 193530) is an autosomal dominant disorder clinically characterized by mild short stature, postaxial polydactyly, nail dystrophy and dysplastic teeth. Ellis-van Creveld syndrome (EvC, MIM 225500) is an autosomal recessive disorder with a similar, but ...

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