Dominant mutations in ROR2, encoding an orphan receptor tyrosine kinase, cause brachydactyly type B
Dominant mutations in ROR2, encoding an orphan receptor tyrosine kinase, cause brachydactyly type B
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New York: Nature Publishing Group US
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English
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New York: Nature Publishing Group US
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Contents
Inherited limb malformations provide a valuable resource for the identification of genes involved in limb development
1
,
2
. Brachydactyly type B (BDB), an autosomal dominant disorder, is the most severe of the brachydactylies
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and characterized by terminal deficiency of the fingers and toes. In the typical form of BDB, the thum...
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Full title
Dominant mutations in ROR2, encoding an orphan receptor tyrosine kinase, cause brachydactyly type B
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TN_cdi_proquest_miscellaneous_70957988
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https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_70957988
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ISSN
1061-4036
E-ISSN
1546-1718
DOI
10.1038/73495
