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European Journal of Medical Genetics|February 16, 2023
Consensus recommendations on altered sensory functioning in Phelan-McDermid syndromeMargreet Walinga, Sarah Jesse, Norma Alhambra, et al.
European Journal of Medical Genetics|April 29, 2023
Parental perspectives on Phelan-McDermid syndrome: Results of a worldwide surveyAnnemiek M Landlust, Sylvia A Koza, Maya Carbin, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 20, 2016
Molecular characterization of NRXN1 deletions from 19,263 clinical microarray cases identifies exons important for neurodevelopmental disease expressionChelsea Lowther, Marsha Speevak, Christine M Armour, et al.
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