177 related articles for article (PubMed ID: 23320815)
1. A study of two Chinese patients with tetrasomy and pentasomy 15q11q13 including Prader-Willi/Angelman syndrome critical region present with developmental delays and mental impairment.
Yang J; Yang Y; Huang Y; Hu Y; Chen X; Sun H; Lv Z; Cheng Q; Bao L
BMC Med Genet; 2013 Jan; 14():9. PubMed ID: 23320815
[TBL] [Abstract][Full Text] [Related]
2. [Analysis of 10 patients with duplications of 15q11q13 region and autism features].
Wang W; Hu C; Bi X; Yuan H
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2018 Feb; 35(1):23-28. PubMed ID: 29419854
[TBL] [Abstract][Full Text] [Related]
3. Clinical and molecular characterization of a large family with an interstitial 15q11q13 duplication.
Piard J; Philippe C; Marvier M; Beneteau C; Roth V; Valduga M; Béri M; Bonnet C; Grégoire MJ; Jonveaux P; Leheup B
Am J Med Genet A; 2010 Aug; 152A(8):1933-41. PubMed ID: 20635369
[TBL] [Abstract][Full Text] [Related]
4. The inv dup (15) or idic (15) syndrome (Tetrasomy 15q).
Battaglia A
Orphanet J Rare Dis; 2008 Nov; 3():30. PubMed ID: 19019226
[TBL] [Abstract][Full Text] [Related]
5. Does parent of origin matter? Methylation studies should be performed on patients with multiple copies of the Prader-Willi/Angelman syndrome critical region.
Aypar U; Brodersen PR; Lundquist PA; Dawson DB; Thorland EC; Hoppman N
Am J Med Genet A; 2014 Oct; 164A(10):2514-20. PubMed ID: 24975781
[TBL] [Abstract][Full Text] [Related]
6. Prader-Willi, Angelman, and 15q11-q13 Duplication Syndromes.
Kalsner L; Chamberlain SJ
Pediatr Clin North Am; 2015 Jun; 62(3):587-606. PubMed ID: 26022164
[TBL] [Abstract][Full Text] [Related]
7. Microdeletion/microduplication of proximal 15q11.2 between BP1 and BP2: a susceptibility region for neurological dysfunction including developmental and language delay.
Burnside RD; Pasion R; Mikhail FM; Carroll AJ; Robin NH; Youngs EL; Gadi IK; Keitges E; Jaswaney VL; Papenhausen PR; Potluri VR; Risheg H; Rush B; Smith JL; Schwartz S; Tepperberg JH; Butler MG
Hum Genet; 2011 Oct; 130(4):517-28. PubMed ID: 21359847
[TBL] [Abstract][Full Text] [Related]
8. Large genomic duplicons map to sites of instability in the Prader-Willi/Angelman syndrome chromosome region (15q11-q13).
Christian SL; Fantes JA; Mewborn SK; Huang B; Ledbetter DH
Hum Mol Genet; 1999 Jun; 8(6):1025-37. PubMed ID: 10332034
[TBL] [Abstract][Full Text] [Related]
9. Interstitial duplications of chromosome region 15q11q13: clinical and molecular characterization.
Repetto GM; White LM; Bader PJ; Johnson D; Knoll JH
Am J Med Genet; 1998 Sep; 79(2):82-9. PubMed ID: 9741464
[TBL] [Abstract][Full Text] [Related]
10. Identification of novel deletions of 15q11q13 in Angelman syndrome by array-CGH: molecular characterization and genotype-phenotype correlations.
Sahoo T; Bacino CA; German JR; Shaw CA; Bird LM; Kimonis V; Anselm I; Waisbren S; Beaudet AL; Peters SU
Eur J Hum Genet; 2007 Sep; 15(9):943-9. PubMed ID: 17522620
[TBL] [Abstract][Full Text] [Related]
11. Genomic imprinting and human chromosome 15.
Repetto GM
Biol Res; 2001; 34(2):141-5. PubMed ID: 11715207
[TBL] [Abstract][Full Text] [Related]
12. Investigation of a cryptic interstitial duplication involving the Prader-Willi/Angelman syndrome critical region.
Thomas NS; Browne CE; Oley C; Healey S; Crolla JA
Hum Genet; 1999 Nov; 105(5):384-7. PubMed ID: 10598802
[TBL] [Abstract][Full Text] [Related]
13. Atypical Prader-Willi and 15q13.3 Microdeletion Syndromes in a Patient with an Unbalanced Translocation.
Colovati MES; Grossi BM; Nunes GD; Fock RA; Guedes DR; Melaragno MI; Cernach MCSP
Cytogenet Genome Res; 2019; 158(4):192-198. PubMed ID: 31394532
[TBL] [Abstract][Full Text] [Related]
14. Multiple forms of atypical rearrangements generating supernumerary derivative chromosome 15.
Wang NJ; Parokonny AS; Thatcher KN; Driscoll J; Malone BM; Dorrani N; Sigman M; LaSalle JM; Schanen NC
BMC Genet; 2008 Jan; 9():2. PubMed ID: 18177502
[TBL] [Abstract][Full Text] [Related]
15. Chromosome 15 uniparental disomy is not frequent in Angelman syndrome.
Knoll JH; Glatt KA; Nicholls RD; Malcolm S; Lalande M
Am J Hum Genet; 1991 Jan; 48(1):16-21. PubMed ID: 1985457
[TBL] [Abstract][Full Text] [Related]
16. Parental Origin of Interstitial Duplications at 15q11.2-q13.3 in Schizophrenia and Neurodevelopmental Disorders.
Isles AR; Ingason A; Lowther C; Walters J; Gawlick M; Stöber G; Rees E; Martin J; Little RB; Potter H; Georgieva L; Pizzo L; Ozaki N; Aleksic B; Kushima I; Ikeda M; Iwata N; Levinson DF; Gejman PV; Shi J; Sanders AR; Duan J; Willis J; Sisodiya S; Costain G; Werge TM; Degenhardt F; Giegling I; Rujescu D; Hreidarsson SJ; Saemundsen E; Ahn JW; Ogilvie C; Girirajan SD; Stefansson H; Stefansson K; O'Donovan MC; Owen MJ; Bassett A; Kirov G
PLoS Genet; 2016 May; 12(5):e1005993. PubMed ID: 27153221
[TBL] [Abstract][Full Text] [Related]
17. Detection of a novel familial deletion of four genes between BP1 and BP2 of the Prader-Willi/Angelman syndrome critical region by oligo-array CGH in a child with neurological disorder and speech impairment.
Murthy SK; Nygren AO; El Shakankiry HM; Schouten JP; Al Khayat AI; Ridha A; Al Ali MT
Cytogenet Genome Res; 2007; 116(1-2):135-40. PubMed ID: 17268193
[TBL] [Abstract][Full Text] [Related]
18. Inherited interstitial duplications of proximal 15q: genotype-phenotype correlations.
Browne CE; Dennis NR; Maher E; Long FL; Nicholson JC; Sillibourne J; Barber JC
Am J Hum Genet; 1997 Dec; 61(6):1342-52. PubMed ID: 9399882
[TBL] [Abstract][Full Text] [Related]
19. Molecular dissection of the Prader-Willi/Angelman syndrome region (15q11-13) by YAC cloning and FISH analysis.
Kuwano A; Mutirangura A; Dittrich B; Buiting K; Horsthemke B; Saitoh S; Niikawa N; Ledbetter SA; Greenberg F; Chinault AC
Hum Mol Genet; 1992 Sep; 1(6):417-25. PubMed ID: 1363801
[TBL] [Abstract][Full Text] [Related]
20. Chromosome 15q11-13 duplication syndrome brain reveals epigenetic alterations in gene expression not predicted from copy number.
Hogart A; Leung KN; Wang NJ; Wu DJ; Driscoll J; Vallero RO; Schanen NC; LaSalle JM
J Med Genet; 2009 Feb; 46(2):86-93. PubMed ID: 18835857
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]