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“22q11.2 Deletion syndrome and obstructive sleep apnea.”, Int J Pediatr Otorhinolaryngol, vol. 78, no. 8, pp. 1360-4, 2014.
, “22q11.2 duplication syndrome: elevated rate of autism spectrum disorder and need for medical screening.”, Mol Autism, vol. 7, p. 27, 2016.
, “Beare-Stevenson syndrome: two new patients, including a novel finding of tracheal cartilaginous sleeve.”, Am J Med Genet A, vol. 167A, no. 4, pp. 852-7, 2015.
, “Contribution of congenital heart disease to neuropsychiatric outcome in school-age children with 22q11.2 deletion syndrome.”, Am J Med Genet B Neuropsychiatr Genet, vol. 165B, no. 2, pp. 137-47, 2014.
, “Critical region within 22q11.2 linked to higher rate of autism spectrum disorder.”, Mol Autism, vol. 8, p. 58, 2017.
, “Disrupted anatomic networks in the 22q11.2 deletion syndrome.”, Neuroimage Clin, vol. 12, pp. 420-8, 2016.
, “Impact of psychiatric comorbidity and cognitive deficit on function in 22q11.2 deletion syndrome.”, J Clin Psychiatry, vol. 76, no. 10, pp. e1262-70, 2015.
, “The Role of mGluR Copy Number Variation in Genetic and Environmental Forms of Syndromic Autism Spectrum Disorder.”, Sci Rep, vol. 6, p. 19372, 2016.
, “Subthreshold psychotic symptoms in 22q11.2 deletion syndrome.”, J Am Acad Child Adolesc Psychiatry, vol. 53, no. 9, pp. 991-1000.e2, 2014.
, “White matter microstructural deficits in 22q11.2 deletion syndrome.”, Psychiatry Res Neuroimaging, vol. 268, pp. 35-44, 2017.
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