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Publications by Dru F. Leistritz
WNT1 Mutations in Families Affected by Moderately Severe and Progressive Recessive Osteogenesis Imperfecta
American Journal of Human Genetics
Genetics
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Splints in Severe Osteogenesis Imperfecta.
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Correction To: Novel Mutation G324C in WNT1 Mapped in a Large Pakistani Family With Severe Recessively Inherited Osteogenesis Imperfecta
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Corrigendum: Prolyl 3-Hydroxylase 1 Deficiency Causes a Recessive Metabolic Bone Disorder Resembling Lethal/Severe Osteogenesis Imperfecta
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Autosomal Recessive Osteogenesis Imperfecta: A Puzzle for Bone Formation, Structure and Function
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