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5.

Recurrent duplications of 17q12 associated with variable phenotypes
by Mitchell, Elyse

American Journal of Medical Genetics. Part A, Dec 2015, Vol.167(12), pp.3038-3045

6.

Investigation of NRXN1 deletions: Clinical and molecular characterization
by Dabell, Mindy Preston

American Journal of Medical Genetics Part A, April 2013, Vol.161(4), pp.717-731

12.

Lymphocytopenia in children with lymphatic malformation.
by Tempero, Richard M

Archives of otolaryngology--head & neck surgery, January 2006, Vol.132(1), pp.93-97

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