Dominant mutations in ROR2, encoding an orphan receptor tyrosine kinase, cause brachydactyly type B (Q28145771)
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scientific article (publication date: March 2000)
Language | Label | Description | Also known as |
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English | Dominant mutations in ROR2, encoding an orphan receptor tyrosine kinase, cause brachydactyly type B |
scientific article (publication date: March 2000) |
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Dominant mutations in ROR2, encoding an orphan receptor tyrosine kinase, cause brachydactyly type B (English)
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March 2000
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