Dominant mutations in ROR2, encoding an orphan receptor tyrosine kinase, cause brachydactyly type B (Q28145771)
scientific article (publication date: March 2000)
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Current Data About Dominant mutations in ROR2, encoding an orphan receptor tyrosine kinase, cause brachydactyly type B
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(P1476) "Dominant mutations in ROR2, encoding an orphan receptor tyrosine kinase, cause brachydactyly type B" (language: en)

(P2093) M Oldridge
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A M Fortuna
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M Maringa
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P Propping
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S Mansour
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C Pollitt
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T M DeChiara
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R B Kimble
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D M Valenzuela
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G D Yancopoulos
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A O Wilkie
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description scientific article (publication date: March 2000)

External Links
(P356) 10.1038/73495
(P698) 10700182
(P6179) 1015891122