Caregivers’ experience of sleep management in Smith–Magenis syndrome: a mixed-methods study

[1] Girirajan S(2006)Genotype-phenotype correlation in Smith–Magenis syndrome: evidence that multiple genes in 17p11.2 contribute to the clinical spectrum Genet Med 8 417-427

[2] Vlangos CN(2003)Refinement of the Smith–Magenis syndrome critical region to approximately 950kb and assessment of 17p11.2 deletions. Are all deletions created equally? Mol Genet Metab 79 134-141

[3] Szomju BB(2012)Smith–Magenis syndrome results in disruption of CLOCK gene transcription and reveals an integral role for RAI1 in the maintenance of circadian rhythmicity Am J Hum Genet 90 941-949

[4] Edelman E(2011)The prevalence and phenomenology of self-injurious and aggressive behaviour in genetic syndromes J Intellect Disabil Res 55 109-120

[5] Trevors CD(1997)Brief report: cognitive and behavioral profiles in persons with Smith-Magenis syndrome J Autism Dev Disord 27 203-211

[6] Dupuis L(2011)Delineation of behavioral phenotypes in genetic syndromes: characteristics of autism spectrum disorder, affect and hyperactivity J Autism Dev Disord 41 1019-1032

[7] Vlangos CN(2016)Differences in social motivation in children with Smith–Magenis syndrome and down syndrome J Autism Dev Disord 46 2148-2159

[8] Yim DKC(2013)The nature of social preference and interactions in Smith–Magenis syndrome Res Dev Disabil 34 4355-4365

[9] Elsea SH(1996)Multi-disciplinary clinical study of Smith–Magenis syndrome (deletion 17p11.2) Am J Med Genet 62 247-254

[10] Williams SR(2001)Abilities and attainment in Smith–Magenis syndrome Dev Med Child Neurol 43 823-828

[1] Girirajan S(2006)Genotype-phenotype correlation in Smith–Magenis syndrome: evidence that multiple genes in 17p11.2 contribute to the clinical spectrum Genet Med 8 417-427

[2] Vlangos CN(2003)Refinement of the Smith–Magenis syndrome critical region to approximately 950kb and assessment of 17p11.2 deletions. Are all deletions created equally? Mol Genet Metab 79 134-141

[3] Szomju BB(2012)Smith–Magenis syndrome results in disruption of CLOCK gene transcription and reveals an integral role for RAI1 in the maintenance of circadian rhythmicity Am J Hum Genet 90 941-949

[4] Edelman E(2011)The prevalence and phenomenology of self-injurious and aggressive behaviour in genetic syndromes J Intellect Disabil Res 55 109-120

[5] Trevors CD(1997)Brief report: cognitive and behavioral profiles in persons with Smith-Magenis syndrome J Autism Dev Disord 27 203-211

[6] Dupuis L(2011)Delineation of behavioral phenotypes in genetic syndromes: characteristics of autism spectrum disorder, affect and hyperactivity J Autism Dev Disord 41 1019-1032

[7] Vlangos CN(2016)Differences in social motivation in children with Smith–Magenis syndrome and down syndrome J Autism Dev Disord 46 2148-2159

[8] Yim DKC(2013)The nature of social preference and interactions in Smith–Magenis syndrome Res Dev Disabil 34 4355-4365

[9] Elsea SH(1996)Multi-disciplinary clinical study of Smith–Magenis syndrome (deletion 17p11.2) Am J Med Genet 62 247-254

[10] Williams SR(2001)Abilities and attainment in Smith–Magenis syndrome Dev Med Child Neurol 43 823-828