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A novel R486Q mutation in BMPR1B resulting in either a brachydactyly type C/symphalangism-like phenotype or brachydactyly type A2
Authors: Lehmann, Katarina; Seemann, Petra; Boergermann, Jan; Morin, Gilles; Reif, Silke; Knaus, Petra; Mundlos, Stefan
Date of Publication (YYYY-MM-DD): 2006-12
Title of Journal: European Journal of Human Genetics
Volume: 14
Issue / Number: 12
Start Page: 1248
End Page: 1254
Document Type: Article
ID: 313090.0
 
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