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dc:description: Orphanet Journal of Rare Diseases 2014, 9:1. doi:10.1186/1750-1172-9-49
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title: X-exome sequencing in Finnish families with Intellectual Disability - four novel mutations and two novel syndromic phenotypes
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dc:title: X-exome sequencing in Finnish families with Intellectual Disability - four novel mutations and two novel syndromic phenotypes
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