WNT1 mutation with recessive osteogenesis imperfecta and profound neurological phenotype. (Q50958600)
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scientific article published on 24 May 2013
Language | Label | Description | Also known as |
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English | WNT1 mutation with recessive osteogenesis imperfecta and profound neurological phenotype. |
scientific article published on 24 May 2013 |
Statements
WNT1 mutation with recessive osteogenesis imperfecta and profound neurological phenotype. (English)
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Fowzan S Alkuraya
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Ranad Shaheen
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Eissa Faqeih
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24 May 2013
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50
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7
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491-492
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