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Further evidence for a parent-of-origin effect at the NOP9 locus on language-related phenotypes
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2 |
Further evidence for a parent-of-origin effect at the NOP9 locus on language-related phenotypes
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BASE
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3 |
Further evidence for a parent-of-origin effect at the NOP9 locus on language-related phenotypes
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BASE
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4 |
Copy Number Variation Screen Identifies a Rare De Novo Deletion at Chromosome 15q13.1-13.3 in a Child with Language Impairment
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BASE
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5 |
Copy number variation screen identifies a rare de novo deletion at chromosome 15q13.1-13.3 in a child with language impairment
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BASE
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6 |
Copy number variation screen identifies a rare de novo deletion at chromosome 15q13.1-13.3 in a child with language impairment
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BASE
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Show details
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