230 related articles for article (PubMed ID: 15979635)
21. Maternal uniparental disomy 14 syndrome demonstrates prader-willi syndrome-like phenotype.
Hosoki K; Kagami M; Tanaka T; Kubota M; Kurosawa K; Kato M; Uetake K; Tohyama J; Ogata T; Saitoh S
J Pediatr; 2009 Dec; 155(6):900-903.e1. PubMed ID: 19800077
[TBL] [Abstract][Full Text] [Related]
22. Maladaptive behavior differences in Prader-Willi syndrome due to paternal deletion versus maternal uniparental disomy.
Dykens EM; Cassidy SB; King BH
Am J Ment Retard; 1999 Jan; 104(1):67-77. PubMed ID: 9972835
[TBL] [Abstract][Full Text] [Related]
23. A rapid microarray based whole genome analysis for detection of uniparental disomy.
Altug-Teber O; Dufke A; Poths S; Mau-Holzmann UA; Bastepe M; Colleaux L; Cormier-Daire V; Eggermann T; Gillessen-Kaesbach G; Bonin M; Riess O
Hum Mutat; 2005 Aug; 26(2):153-9. PubMed ID: 15968682
[TBL] [Abstract][Full Text] [Related]
24. Comparison of phenotype between patients with Prader-Willi syndrome due to deletion 15q and uniparental disomy 15.
Cassidy SB; Forsythe M; Heeger S; Nicholls RD; Schork N; Benn P; Schwartz S
Am J Med Genet; 1997 Feb; 68(4):433-40. PubMed ID: 9021017
[TBL] [Abstract][Full Text] [Related]
25. Genetic Subtype-Phenotype Analysis of Growth Hormone Treatment on Psychiatric Behavior in Prader-Willi Syndrome.
Montes AS; Osann KE; Gold JA; Tamura RN; Driscoll DJ; Butler MG; Kimonis VE
Genes (Basel); 2020 Oct; 11(11):. PubMed ID: 33114160
[TBL] [Abstract][Full Text] [Related]
26. Validation studies of SNRPN methylation as a diagnostic test for Prader-Willi syndrome.
Kubota T; Sutcliffe JS; Aradhya S; Gillessen-Kaesbach G; Christian SL; Horsthemke B; Beaudet AL; Ledbetter DH
Am J Med Genet; 1996 Dec; 66(1):77-80. PubMed ID: 8957518
[TBL] [Abstract][Full Text] [Related]
27. Molecular diagnosis of Prader-Willi syndrome.
Pangkanon S
J Med Assoc Thai; 2003 Aug; 86 Suppl 3():S510-6. PubMed ID: 14700141
[TBL] [Abstract][Full Text] [Related]
28. Delayed diagnosis in patients with Prader-Willi syndrome due to maternal uniparental disomy 15.
Gunay-Aygun M; Heeger S; Schwartz S; Cassidy SB
Am J Med Genet; 1997 Jul; 71(1):106-10. PubMed ID: 9215778
[TBL] [Abstract][Full Text] [Related]
29. The contribution of uniparental disomy to congenital development defects in children born to mothers at advanced childbearing age.
Ginsburg C; Fokstuen S; Schinzel A
Am J Med Genet; 2000 Dec; 95(5):454-60. PubMed ID: 11146466
[TBL] [Abstract][Full Text] [Related]
30. 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
Am J Med Genet; 1997 Jan; 68(2):195-206. PubMed ID: 9028458
[TBL] [Abstract][Full Text] [Related]
31. Visualization of uniparental inheritance, Mendelian inconsistencies, deletions, and parent of origin effects in single nucleotide polymorphism trio data with SNPtrio.
Ting JC; Roberson ED; Miller ND; Lysholm-Bernacchi A; Stephan DA; Capone GT; Ruczinski I; Thomas GH; Pevsner J
Hum Mutat; 2007 Dec; 28(12):1225-35. PubMed ID: 17661425
[TBL] [Abstract][Full Text] [Related]
32. Maternal age effect on the development of Prader-Willi syndrome resulting from upd(15)mat through meiosis 1 errors.
Matsubara K; Murakami N; Nagai T; Ogata T
J Hum Genet; 2011 Aug; 56(8):566-71. PubMed ID: 21633360
[TBL] [Abstract][Full Text] [Related]
33. A case described as translocation 15;15 revised: maternal 15 UPD, resulting from isochromosome 15, in a PWS patient.
Gutkowska A; Tylki-Szymańska A; Popowska E; Bielińska B; Jurkiewicz D; Krajewska-Walasek M
Eur J Med Genet; 2005; 48(2):207-9. PubMed ID: 16053914
[No Abstract] [Full Text] [Related]
34. Genetics and mathematics: evidence from Prader-Willi syndrome.
Semenza C; Pignatti R; Bertella L; Ceriani F; Mori I; Molinari E; Giardino D; Malvestiti F; Grugni G
Neuropsychologia; 2008 Jan; 46(1):206-12. PubMed ID: 17845808
[TBL] [Abstract][Full Text] [Related]
35. Prenatal diagnosis of Prader-Willi syndrome due to uniparental disomy with NIPS: Case report and literature review.
Shubina J; Barkov IY; Stupko OK; Kuznetsova MV; Goltsov AY; Kochetkova TO; Trofimov DY; Sukhikh GT
Mol Genet Genomic Med; 2020 Oct; 8(10):e1448. PubMed ID: 32857485
[TBL] [Abstract][Full Text] [Related]
36. Genetic subtypes and phenotypic characteristics of 110 patients with Prader-Willi syndrome.
Zhang L; Liu X; Zhao Y; Wang Q; Zhang Y; Gao H; Zhang B; Cui W; Zhao Y
Ital J Pediatr; 2022 Jul; 48(1):121. PubMed ID: 35870983
[TBL] [Abstract][Full Text] [Related]
37. CD36 expression and its relationship with obesity in blood cells from people with and without Prader-Willi syndrome.
Webb T; Whittington J; Holland AJ; Soni S; Boer H; Clarke D; Horsthemke B
Clin Genet; 2006 Jan; 69(1):26-32. PubMed ID: 16451133
[TBL] [Abstract][Full Text] [Related]
38. Genetic basis of Prader-Willi syndrome in Korea: less uniparental disomy than has been recognized?
Kim HJ; Cho HJ; Jin DK; Kwon EK; Ki CS; Kim JW; Kim SH
Clin Genet; 2004 Oct; 66(4):368-72. PubMed ID: 15355442
[No Abstract] [Full Text] [Related]
39. Ageing in people with Prader-Willi syndrome: mortality in the UK population cohort and morbidity in an older sample of adults.
Whittington JE; Holland AJ; Webb T
Psychol Med; 2015 Feb; 45(3):615-21. PubMed ID: 25088280
[TBL] [Abstract][Full Text] [Related]
40. Death in adults with Prader-Willi syndrome may be correlated with maternal uniparental disomy.
Smith A; Loughnan G; Steinbeck K
J Med Genet; 2003 May; 40(5):e63. PubMed ID: 12746417
[No Abstract] [Full Text] [Related]
[Previous] [Next] [New Search]