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Dive into the research topics of 'Novel deletion of SERPINF1 causes autosomal recessive osteogenesis imperfecta type VI in two Brazilian families'. Together they form a unique fingerprint.- Sort by
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Renata Moldenhauer Minillo, Nara Sobreira, Maria De Fatima De Faria Soares, Julie Jurgens, Hua Ling, Kurt N. Hetrick, Kimberly F. Doheny, David Valle, Decio Brunoni, Ana B.Alvarez Perez
Research output: Contribution to journal › Article › peer-review