Angelman, Harry (1965). “'Puppet' Children: A report of three cases”. 《Dev Med Child Neurol》 7 (6): 681–688. doi:10.1111/j.1469-8749.1965.tb07844.x.
Weeber E, Levenson J, Sweatt J (2002). “Molecular genetics of human cognition”. 《Mol Interv》 2 (6): 376–91, 339. doi:10.1124/mi.2.6.376. PMID14993414.
White HE, Durston VJ, Harvey JF, Cross NC (2006). “Quantitative analysis of SNRPN(correction of SRNPN) gene methylation by pyrosequencing as a diagnostic test for Prader-Willi syndrome and Angelman syndrome”. 《Clin. Chem.》 52 (6): 1005–13. doi:10.1373/clinchem.2005.065086. PMID16574761.
Leung, HT; Ring, H (January 2013). “Epilepsy in four genetically determined syndromes of intellectual disability.”. 《Journal of intellectual disability research : JIDR》 57 (1): 3–20. doi:10.1111/j.1365-2788.2011.01505.x. PMID22142420.
Andersen WH, Rasmussen RK, Strømme P (2001). “Levels of cognitive and linguistic development in Angelman syndrome: a study of 20 children”. 《Logopedics, Phoniatrics, Vocology》 26 (1): 2–9. doi:10.1080/140154301300109044. PMID11432411.
Steffenburg S, Gillberg CL, Steffenburg U, Kyllerman M (1996). “Autism in Angelman syndrome: a population-based study”. 《Pediatr. Neurol.》 14 (2): 131–6. doi:10.1016/0887-8994(96)00011-2. PMID8703225.
Petersen MB, Brøndum-Nielsen K, Hansen LK, Wulff K (1995). “Clinical, cytogenetic, and molecular diagnosis of Angelman syndrome: estimated prevalence rate in a Danish county; the disorder predominantly affects Anglo-Saxons”. 《Am. J. Med. Genet.》 60 (3): 261–2. doi:10.1002/ajmg.1320600317. PMID7573182.
Galassi FM, Armocida E, Rühli FJ (September 2016). “Angelman Syndrome in the Portrait of a Child With a Drawing by Giovanni F. Caroto”. 《JAMA Pediatr》 170 (9): 831. doi:10.1001/jamapediatrics.2016.0581. PMID27380555.
Magenis, RE; Brown MG; Lacy DA; Budden S; LaFranchi S. (1987). “Is Angelman syndrome an alternate result of del(15)(q11q13)?”. 《Am J Med Genet》 28 (4): 829–38. doi:10.1002/ajmg.1320280407. PMID3688021.
Weeber E, Levenson J, Sweatt J (2002). “Molecular genetics of human cognition”. 《Mol Interv》 2 (6): 376–91, 339. doi:10.1124/mi.2.6.376. PMID14993414.
White HE, Durston VJ, Harvey JF, Cross NC (2006). “Quantitative analysis of SNRPN(correction of SRNPN) gene methylation by pyrosequencing as a diagnostic test for Prader-Willi syndrome and Angelman syndrome”. 《Clin. Chem.》 52 (6): 1005–13. doi:10.1373/clinchem.2005.065086. PMID16574761.
Leung, HT; Ring, H (January 2013). “Epilepsy in four genetically determined syndromes of intellectual disability.”. 《Journal of intellectual disability research : JIDR》 57 (1): 3–20. doi:10.1111/j.1365-2788.2011.01505.x. PMID22142420.
Andersen WH, Rasmussen RK, Strømme P (2001). “Levels of cognitive and linguistic development in Angelman syndrome: a study of 20 children”. 《Logopedics, Phoniatrics, Vocology》 26 (1): 2–9. doi:10.1080/140154301300109044. PMID11432411.
Steffenburg S, Gillberg CL, Steffenburg U, Kyllerman M (1996). “Autism in Angelman syndrome: a population-based study”. 《Pediatr. Neurol.》 14 (2): 131–6. doi:10.1016/0887-8994(96)00011-2. PMID8703225.
Petersen MB, Brøndum-Nielsen K, Hansen LK, Wulff K (1995). “Clinical, cytogenetic, and molecular diagnosis of Angelman syndrome: estimated prevalence rate in a Danish county; the disorder predominantly affects Anglo-Saxons”. 《Am. J. Med. Genet.》 60 (3): 261–2. doi:10.1002/ajmg.1320600317. PMID7573182.
Galassi FM, Armocida E, Rühli FJ (September 2016). “Angelman Syndrome in the Portrait of a Child With a Drawing by Giovanni F. Caroto”. 《JAMA Pediatr》 170 (9): 831. doi:10.1001/jamapediatrics.2016.0581. PMID27380555.
Magenis, RE; Brown MG; Lacy DA; Budden S; LaFranchi S. (1987). “Is Angelman syndrome an alternate result of del(15)(q11q13)?”. 《Am J Med Genet》 28 (4): 829–38. doi:10.1002/ajmg.1320280407. PMID3688021.
ghr.nlm.nih.gov
Reference, Genetics Home (May 2015). “Angelman syndrome”. 《Genetics Home Reference》. 27 August 2016에 원본 문서에서 보존된 문서. 28 April 2017에 확인함.