Image of the Month: Answer
- 卷第46卷
- 印刷ISSN1034-4810
- 电子ISSN1440-1754
- 文件大小95.30KB
- 发表时间2010
- DOI10.1111/j.1440-1754.2009.01703_2.x
- 页码69-69
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Genetic variation affecting DNA methylation and the human imprinting disorder, Beckwith-Wiedemann syndromeDagar, Vinod; Hutchison, Wendy; Muscat, Andrea; Krishnan, Anita; Hoke, David; Buckle, Ashley; Siswara, Priscillia; Amor, David J.; Mann, Jeffrey; Pinner, Jason; Colley, Alison; Wilson, Meredith; Sachdev, Rani; McGillivray, George; Edwards, Matthew; Kirk, Edwin; Collins, Felicity; Jones, Kristi; Taylor, Juliet; Hayes, Ian; Thompson, Elizabeth; Barnett, Christopher; Haan, Eric; Freckmann, Mary-Louise; Turner, Anne; White, Susan; Kamien, Ben; Ma, Alan; Mackenzie, Fiona; Baynam, Gareth; Kiraly-Borri, Cathy; Field, Michael; Dudding-Byth, Tracey; Algar, Elizabeth M. · Clinical Epigenetics · 2018
Characterization of a 520 kb deletion on chromosome 15q26.1 including <i>ST8SIA2</i> in a patient with behavioral disturbance, autism spectrum disorder, and epilepsyKamien, Benjamin; Harraway, James; Lundie, Ben; Smallhorne, Lex; Gibbs, Vicki; Heath, Anna; Fullerton, Janice M. · American Journal of Medical Genetics Part A · 2014
Characterization of a 520 kb deletion on chromosome 15q26.1 including <i>ST8SIA2</i> in a patient with behavioral disturbance, autism spectrum disorder, and epilepsy: Additional informationKamien, Benjamin; Harraway, James; Lundie, Ben; Smallhorne, Lex; Gibbs, Vicki; Heath, Anna; Fullerton, Janice M. · American Journal of Medical Genetics Part A · 2015