WNT1 mutation with recessive osteogenesis imperfecta and profound neurological phenotype | Journal of Medical Genetics

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WNT1 mutation with recessive osteogenesis imperfecta and profound neurological phenotype

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Cite this article as:: Faqeih E, Shaheen R, Alkuraya FS

WNT1 mutation with recessive osteogenesis imperfecta and profound neurological phenotype

Journal of Medical Genetics 2013;50:491-492.