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22. Chromatin acetylation, memory, and LTP are impaired in CBP+/- mice: a model for the cognitive deficit in Rubinstein-Taybi syndrome and its amelioration. Alarcón JM; Malleret G; Touzani K; Vronskaya S; Ishii S; Kandel ER; Barco A Neuron; 2004 Jun; 42(6):947-59. PubMed ID: 15207239 [TBL] [Abstract][Full Text] [Related]
23. Rubinstein-Taybi syndrome and CREBBP c.201 202delTA mutation: a case presenting with varicella meningoencephalitis. Çaksen H; Bartsch O; Okur M; Temel H; Açikgoz M; Yilmaz C Genet Couns; 2009; 20(3):255-60. PubMed ID: 19852432 [TBL] [Abstract][Full Text] [Related]
24. Molecular analysis of the CBP gene in 60 patients with Rubinstein-Taybi syndrome. Coupry I; Roudaut C; Stef M; Delrue MA; Marche M; Burgelin I; Taine L; Cruaud C; Lacombe D; Arveiler B J Med Genet; 2002 Jun; 39(6):415-21. PubMed ID: 12070251 [No Abstract] [Full Text] [Related]
25. CREBBP mutations in individuals without Rubinstein-Taybi syndrome phenotype. Menke LA; van Belzen MJ; Alders M; Cristofoli F; ; Ehmke N; Fergelot P; Foster A; Gerkes EH; Hoffer MJ; Horn D; Kant SG; Lacombe D; Leon E; Maas SM; Melis D; Muto V; Park SM; Peeters H; Peters DJ; Pfundt R; van Ravenswaaij-Arts CM; Tartaglia M; Hennekam RC Am J Med Genet A; 2016 Oct; 170(10):2681-93. PubMed ID: 27311832 [TBL] [Abstract][Full Text] [Related]
26. [CREBBP gene mutation in two boys with Rubinstein-Taybi syndrome]. Zhang J; Wang C; Li M; Qiu Z Zhonghua Er Ke Za Zhi; 2014 Sep; 52(9):673-7. PubMed ID: 25476429 [TBL] [Abstract][Full Text] [Related]
27. Evidence for a new contiguous gene syndrome, the chromosome 16p13.3 deletion syndrome alias severe Rubinstein-Taybi syndrome. Bartsch O; Rasi S; Delicado A; Dyack S; Neumann LM; Seemanová E; Volleth M; Haaf T; Kalscheuer VM Hum Genet; 2006 Sep; 120(2):179-86. PubMed ID: 16783566 [TBL] [Abstract][Full Text] [Related]
28. Letter to the Editor: A Novel Mutation in the CREBBP Gene of a Korean Girl with Rubinstein-Taybi syndrome. Huh R; Cho SY; Kim J; Ki CS; Jin DK Ann Clin Lab Sci; 2015; 45(4):458-61. PubMed ID: 26275701 [TBL] [Abstract][Full Text] [Related]
29. [Clinical sequelae of mutation of the CBP gene]. Smardová J; Smarda J Cas Lek Cesk; 1999 Dec; 138(24):739-43. PubMed ID: 10746038 [TBL] [Abstract][Full Text] [Related]
30. Rubinstein-Taybi syndrome with normal FISH result and CREBBP gene analysis: a case report. Balci S; Ergün MA; Yüksel-Konuk EB; Bartsch O Turk J Pediatr; 2008; 50(3):265-8. PubMed ID: 18773673 [TBL] [Abstract][Full Text] [Related]
31. A boy with classical Rubinstein-Taybi syndrome but no detectable mutation in the CREBBP and EP300 genes. Caglayan AO; Lechno S; Gumus H; Bartsch O; Fryns JP Genet Couns; 2011; 22(4):341-6. PubMed ID: 22303793 [TBL] [Abstract][Full Text] [Related]
32. Genetic heterogeneity in Rubinstein-Taybi syndrome: mutations in both the CBP and EP300 genes cause disease. Roelfsema JH; White SJ; Ariyürek Y; Bartholdi D; Niedrist D; Papadia F; Bacino CA; den Dunnen JT; van Ommen GJ; Breuning MH; Hennekam RC; Peters DJ Am J Hum Genet; 2005 Apr; 76(4):572-80. PubMed ID: 15706485 [TBL] [Abstract][Full Text] [Related]
33. Exon deletions of the EP300 and CREBBP genes in two children with Rubinstein-Taybi syndrome detected by aCGH. Tsai AC; Dossett CJ; Walton CS; Cramer AE; Eng PA; Nowakowska BA; Pursley AN; Stankiewicz P; Wiszniewska J; Cheung SW Eur J Hum Genet; 2011 Jan; 19(1):43-9. PubMed ID: 20717166 [TBL] [Abstract][Full Text] [Related]
34. Rubinstein-Taybi syndrome and familial Mediterranean fever in a single patient: two distinct genetic diseases located on chromosome 16p13.3. Kalyoncu U; Tufan A; Karadag O; Kisacik B; Akdogan A; Calguneri M J Natl Med Assoc; 2006 Oct; 98(10):1692-3. PubMed ID: 17052063 [TBL] [Abstract][Full Text] [Related]
35. A mouse model of Rubinstein-Taybi syndrome: defective long-term memory is ameliorated by inhibitors of phosphodiesterase 4. Bourtchouladze R; Lidge R; Catapano R; Stanley J; Gossweiler S; Romashko D; Scott R; Tully T Proc Natl Acad Sci U S A; 2003 Sep; 100(18):10518-22. PubMed ID: 12930888 [TBL] [Abstract][Full Text] [Related]
37. Rubinstein-Taybi syndrome type 2: report of nine new cases that extend the phenotypic and genotypic spectrum. Hamilton MJ; Newbury-Ecob R; Holder-Espinasse M; Yau S; Lillis S; Hurst JA; Clement E; Reardon W; Joss S; Hobson E; Blyth M; Al-Shehhi M; Lynch SA; Suri M; Clin Dysmorphol; 2016 Oct; 25(4):135-45. PubMed ID: 27465822 [TBL] [Abstract][Full Text] [Related]
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40. [Clinical and genetic analysis of two cases with Rubinstein-Taybi syndrome]. Tang F; Li Z; Cheng X; Su N; Yan L; Gou P; Gong C Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2019 Sep; 36(9):886-889. PubMed ID: 31515782 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]