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2. Clinical features associated with copy number variations of the 14q32 imprinted gene cluster. (26th November 2014)

3. Investigation of NRXN1 deletions: Clinical and molecular characterization12. Issue 4 (12th March 2013)

4. Phenotypic and molecular characterization of 19q12q13.1 deletions: A report of five patients. Issue 1 (15th November 2013)