These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
132 related articles for article (PubMed ID: 35600042)
1. Complex chromosomal rearrangement involving 15q11-q13 interstitial triplication and duplication: A new case report of dysmorphic and neuropsychiatric features. Chilakamarri L; Mellin-Sanchez EL Clin Case Rep; 2022 May; 10(5):e05835. PubMed ID: 35600042 [TBL] [Abstract][Full Text] [Related]
2. Complex de novo chromosomal rearrangement at 15q11-q13 involving an intrachromosomal triplication in a patient with a severe neuropsychological phenotype: clinical report and review of the literature. Castronovo C; Crippa M; Bestetti I; Rusconi D; Russo S; Larizza L; Sangermani R; Bonati MT; Finelli P Am J Med Genet A; 2015 Jan; 167A(1):221-30. PubMed ID: 25339188 [TBL] [Abstract][Full Text] [Related]
3. Complete Penetrance but Different Phenotypes in a Korean Family with Maternal Interstitial Duplication at 15q11.2-q13.1: A Case Report. Han JY; Lee HJ; Lee YM; Park J Children (Basel); 2021 Apr; 8(4):. PubMed ID: 33924158 [TBL] [Abstract][Full Text] [Related]
4. De novo interstitial duplication of 15q11.2-q13.1 with complex maternal uniparental trisomy for the 15q11-q13 region in a patient with Prader-Willi syndrome. Burrage LC; Person RE; Flores A; Villanos MT; Bi W; Wiszniewska J; Bacino CA Am J Med Genet A; 2012 Oct; 158A(10):2557-63. PubMed ID: 22903639 [TBL] [Abstract][Full Text] [Related]
5. Molecular characterisation of four cases of intrachromosomal triplication of chromosome 15q11-q14. Ungaro P; Christian SL; Fantes JA; Mutirangura A; Black S; Reynolds J; Malcolm S; Dobyns WB; Ledbetter DH J Med Genet; 2001 Jan; 38(1):26-34. PubMed ID: 11134237 [TBL] [Abstract][Full Text] [Related]
6. 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]
8. Screening for genomic rearrangements and methylation abnormalities of the 15q11-q13 region in autism spectrum disorders. Depienne C; Moreno-De-Luca D; Heron D; Bouteiller D; Gennetier A; Delorme R; Chaste P; Siffroi JP; Chantot-Bastaraud S; Benyahia B; Trouillard O; Nygren G; Kopp S; Johansson M; Rastam M; Burglen L; Leguern E; Verloes A; Leboyer M; Brice A; Gillberg C; Betancur C Biol Psychiatry; 2009 Aug; 66(4):349-59. PubMed ID: 19278672 [TBL] [Abstract][Full Text] [Related]
9. A case of 15q11-q13 duplication syndrome and literature review. Fu Z; Jia YX; Fu JX; Li TX; Zhao JJ; Wang T; Qiao ZD; Liu XY; Tang R; Lv T; Yang GL Brain Behav; 2021 Aug; 11(8):e2219. PubMed ID: 34292674 [TBL] [Abstract][Full Text] [Related]
10. Gene expression analysis of human induced pluripotent stem cell-derived neurons carrying copy number variants of chromosome 15q11-q13.1. Germain ND; Chen PF; Plocik AM; Glatt-Deeley H; Brown J; Fink JJ; Bolduc KA; Robinson TM; Levine ES; Reiter LT; Graveley BR; Lalande M; Chamberlain SJ Mol Autism; 2014; 5():44. PubMed ID: 25694803 [TBL] [Abstract][Full Text] [Related]
13. 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]
14. A Rare Inherited 15q11.2-q13.1 Interstitial Duplication with Maternal Somatic Mosaicism, Renal Carcinoma, and Autism. Urraca N; Potter B; Hundley R; Pivnick EK; McVicar K; Thibert RL; Ledbetter C; Chamberlain R; Miravalle L; Sirois CL; Chamberlain S; Reiter LT Front Genet; 2016; 7():205. PubMed ID: 27933089 [TBL] [Abstract][Full Text] [Related]
15. Duplication of the 15q11-q13 region: clinical and genetic study of 30 new cases. Al Ageeli E; Drunat S; Delanoë C; Perrin L; Baumann C; Capri Y; Fabre-Teste J; Aboura A; Dupont C; Auvin S; El Khattabi L; Chantereau D; Moncla A; Tabet AC; Verloes A Eur J Med Genet; 2014 Jan; 57(1):5-14. PubMed ID: 24239951 [TBL] [Abstract][Full Text] [Related]
16. De novo interstitial duplication of the 15q11.2-q14 PWS/AS region of maternal origin: Clinical description, array CGH analysis, and review of the literature. Kitsiou-Tzeli S; Tzetis M; Sofocleous C; Vrettou C; Xaidara A; Giannikou K; Pampanos A; Mavrou A; Kanavakis E Am J Med Genet A; 2010 Aug; 152A(8):1925-32. PubMed ID: 20575009 [TBL] [Abstract][Full Text] [Related]
17. Neurological features and long-term follow-up in 15q11.2-13.1 duplication. Coppola A; Ruosi P; Santulli L; Striano S; Zara F; Striano P; Sisodiya SM Eur J Med Genet; 2013 Nov; 56(11):614-8. PubMed ID: 24075935 [TBL] [Abstract][Full Text] [Related]
18. 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]
19. Rare partial trisomy and tetrasomy of 15q11-q13 associated with developmental delay and autism spectrum disorder. Lu Y; Liang Y; Ning S; Deng G; Xie Y; Song J; Zuo N; Feng C; Qin Y Mol Cytogenet; 2020; 13():21. PubMed ID: 32536972 [TBL] [Abstract][Full Text] [Related]