How to cite this article: Millson A, LaGrave D, Willis MJH, Rowe LR, Lyon E, South ST. 2012. Chromosomal loss of 3q26.3-3q26.32, involving a partial neuroligin 1 deletion, identified by genomic microarray in a child with microcephaly, seizure disorder, and severe intellectual disability. Am J Med Genet Part A 158A:159–165.
Clinical Report
Chromosomal loss of 3q26.3-3q26.32, involving a partial neuroligin 1 deletion, identified by genomic microarray in a child with microcephaly, seizure disorder, and severe intellectual disability†‡
Article first published online: 21 NOV 2011
DOI: 10.1002/ajmg.a.34349
Copyright © 2011 Wiley Periodicals, Inc.
Additional Information
How to Cite
Millson, A., LaGrave, D., Willis, M. J.H., Rowe, L. R., Lyon, E. and South, S. T. (2012), Chromosomal loss of 3q26.3-3q26.32, involving a partial neuroligin 1 deletion, identified by genomic microarray in a child with microcephaly, seizure disorder, and severe intellectual disability. Am. J. Med. Genet., 158A: 159–165. doi: 10.1002/ajmg.a.34349
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The views expressed in this article are those of the authors and do not necessarily reflect the official policy or position of the Department of the Navy, Department of Defense, or the United States Government.
Publication History
- Issue published online: 19 DEC 2011
- Article first published online: 21 NOV 2011
- Manuscript Accepted: 22 SEP 2011
- Manuscript Received: 22 FEB 2011
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