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- W2187447310 abstract "Osteogenesis Imperfecta (OI) is a group of inherited disorders characterized by bone fragility. The perinatal lethal form of the disease, type II, has three different mechanisms of inheritance: new dominant mutations, parental germline mosaicism, and autosomal recessive inheritance. We present a case of recurrent OI type II to discuss evolving aspects of diagnosis and to highlight the unique challenges faced when counseling patients." @default.
- W2187447310 created "2016-06-24" @default.
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- W2187447310 date "2014-01-01" @default.
- W2187447310 modified "2023-09-27" @default.
- W2187447310 title "Recurrent Osteogenesis Imperfecta" @default.
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