BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

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]
    of 12.