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Prader-Willi and Angelman syndromes: sister imprinted disorders.
Cassidy SB, Dykens E, Williams CA. Cassidy SB, et al. Among authors: williams ca. Am J Med Genet. 2000 Summer;97(2):136-46. doi: 10.1002/1096-8628(200022)97:2<136::aid-ajmg5>3.0.co;2-v. Am J Med Genet. 2000. PMID: 11180221 Review.
Clinical spectrum and molecular diagnosis of Angelman and Prader-Willi syndrome patients with an imprinting mutation.
Saitoh S, Buiting K, Cassidy SB, Conroy JM, Driscoll DJ, Gabriel JM, Gillessen-Kaesbach G, Glenn CC, Greenswag LR, Horsthemke B, Kondo I, Kuwajima K, Niikawa N, Rogan PK, Schwartz S, Seip J, Williams CA, Nicholls RD. Saitoh S, et al. Among authors: williams ca. Am J Med Genet. 1997 Jan 20;68(2):195-206. Am J Med Genet. 1997. PMID: 9028458
Distinct phenotypes distinguish the molecular classes of Angelman syndrome.
Lossie AC, Whitney MM, Amidon D, Dong HJ, Chen P, Theriaque D, Hutson A, Nicholls RD, Zori RT, Williams CA, Driscoll DJ. Lossie AC, et al. Among authors: williams ca. J Med Genet. 2001 Dec;38(12):834-45. doi: 10.1136/jmg.38.12.834. J Med Genet. 2001. PMID: 11748306 Free PMC article.
Clinical and genetic aspects of Angelman syndrome.
Williams CA, Driscoll DJ, Dagli AI. Williams CA, et al. Genet Med. 2010 Jul;12(7):385-95. doi: 10.1097/GIM.0b013e3181def138. Genet Med. 2010. PMID: 20445456 Free article. Review.
748 results