Similar articles for PMID: 10424818

Year	Number of Results
1989	1
1993	3
1994	4
1995	1
1996	3
1997	11
1998	12
1999	13
2000	3
2001	6
2002	4
2003	7
2004	9
2005	8
2006	6
2007	5
2008	5
2009	8
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2011	9
2012	7
2013	14
2014	16
2015	11
2016	14
2017	12
2018	2
2019	10
2020	12
2021	8
2022	12
2023	3
2024	2

1

Angelman syndrome resulting from UBE3A mutations in 14 patients from eight families: clinical manifestations and genetic counselling.

Moncla A, Malzac P, Livet MO, Voelckel MA, Mancini J, Delaroziere JC, Philip N, Mattei JF. Moncla A, et al. J Med Genet. 1999 Jul;36(7):554-60. J Med Genet. 1999. PMID: 10424818 Free PMC article.

2

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. 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.

3

Mutation analysis of UBE3A in Angelman syndrome patients.

Malzac P, Webber H, Moncla A, Graham JM, Kukolich M, Williams C, Pagon RA, Ramsdell LA, Kishino T, Wagstaff J. Malzac P, et al. Am J Hum Genet. 1998 Jun;62(6):1353-60. doi: 10.1086/301877. Am J Hum Genet. 1998. PMID: 9585605 Free PMC article.

4

The spectrum of mutations in UBE3A causing Angelman syndrome.

Fang P, Lev-Lehman E, Tsai TF, Matsuura T, Benton CS, Sutcliffe JS, Christian SL, Kubota T, Halley DJ, Meijers-Heijboer H, Langlois S, Graham JM Jr, Beuten J, Willems PJ, Ledbetter DH, Beaudet AL. Fang P, et al. Hum Mol Genet. 1999 Jan;8(1):129-35. doi: 10.1093/hmg/8.1.129. Hum Mol Genet. 1999. PMID: 9887341

5

UBE3A/E6-AP mutations cause Angelman syndrome.

Kishino T, Lalande M, Wagstaff J. Kishino T, et al. Nat Genet. 1997 Jan;15(1):70-3. doi: 10.1038/ng0197-70. Nat Genet. 1997. PMID: 8988171

6

Angelman Syndrome due to a Maternally Inherited Intragenic Deletion Encompassing Exons 7 and 8 of the UBE3A Gene.

Ververi A, Islam L, Bewes B, Busby L, Sullivan C, Canham N. Ververi A, et al. Cytogenet Genome Res. 2017;152(3):132-136. doi: 10.1159/000480030. Epub 2017 Sep 13. Cytogenet Genome Res. 2017. PMID: 28898887

7

Angelman syndrome: a review of the clinical and genetic aspects.

Clayton-Smith J, Laan L. Clayton-Smith J, et al. J Med Genet. 2003 Feb;40(2):87-95. doi: 10.1136/jmg.40.2.87. J Med Genet. 2003. PMID: 12566516 Free PMC article. Review.

8

UBE3A gene mutations in Finnish Angelman syndrome patients detected by conformation sensitive gel electrophoresis.

Rapakko K, Kokkonen H, Leisti J. Rapakko K, et al. Am J Med Genet A. 2004 Apr 30;126A(3):248-52. doi: 10.1002/ajmg.a.20587. Am J Med Genet A. 2004. PMID: 15054837

9

Investigation of UBE3A and MECP2 in Angelman syndrome (AS) and patients with features of AS.

Hitchins MP, Rickard S, Dhalla F, Fairbrother UL, de Vries BB, Winter R, Pembrey ME, Malcolm S. Hitchins MP, et al. Am J Med Genet A. 2004 Mar 1;125A(2):167-72. doi: 10.1002/ajmg.a.20343. Am J Med Genet A. 2004. PMID: 14981718

10

Angelman syndrome: etiology, clinical features, diagnosis, and management of symptoms.

Guerrini R, Carrozzo R, Rinaldi R, Bonanni P. Guerrini R, et al. Paediatr Drugs. 2003;5(10):647-61. doi: 10.2165/00148581-200305100-00001. Paediatr Drugs. 2003. PMID: 14510623 Review.

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