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Your search keyword '"Moosa, Shahida"' showing total 3 results

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3 results on '"Moosa, Shahida"'

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1. Null and missense mutations of ERI1 cause a recessive phenotypic dichotomy in humans

2. Autosomal-Recessive Mutations in MESD Cause Osteogenesis Imperfecta

3. Mutations in CKAP2L, the Human Homolog of the Mouse Radmis Gene, Cause Filippi Syndrome

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