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Dive into the research topics of 'Copy number variation screen identifies a rare de Novo deletion at chromosome 15q13.1-13.3 in a child with language impairment'. Together they form a unique fingerprint.- Sort by
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Kerry A. Pettigrew, Emily Reeves, Ruth Leavett, Marianna E. Hayiou-Thomas, Anahita Sharma, Nuala H. Simpson, Angela Martinelli, Paul Thompson, Charles Hulme, Margaret J. Snowling, Dianne F. Newbury, Silvia Paracchini
Research output: Contribution to journal › Article › peer-review