21 |
Further evidence for a parent-of-origin effect at the NOP9 locus on language-related phenotypes
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22 |
Further evidence for a parent-of-origin effect at the NOP9 locus on language-related phenotypes
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23 |
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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25 |
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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26 |
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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27 |
Genome-wide screening for DNA variants associated with reading and language traits
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28 |
Genome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairment
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29 |
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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30 |
Reading and language disorders : the importance of both quantity and quality
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31 |
Associations of HLA alleles with specific language impairment
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32 |
Homozygous microdeletion of exon 5 in ZNF277 in a girl with specific language impairment.
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33 |
Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia.
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34 |
Associations of HLA alleles with specific language impairment
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35 |
Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia
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36 |
Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia
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BASE
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37 |
Genome-wide analysis of genetic susceptibility to language impairment in an isolated Chilean population
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39 |
CMIP and ATP2C2 Modulate Phonological Short-Term Memory in Language Impairment
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40 |
CMIP and ATP2C2 modulate phonological short-term memory in language impairment
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