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42. Inheritance of Rubinstein-Taybi syndrome. Bonioli E; Bellini C Am J Med Genet; 1989 Apr; 32(4):559. PubMed ID: 2774008 [No Abstract] [Full Text] [Related]
43. New CBP mutations in Brazilian patients with Rubinstein-Taybi syndrome. Suzuki KT; Torres LC; Sugayama SM; Aguiar Alves Bda C; Moreira-Filho CA; Carneiro-Sampaio M Clin Genet; 2013 Mar; 83(3):291-2. PubMed ID: 22591219 [No Abstract] [Full Text] [Related]
44. A patient with a de-novo deletion 3p25.3 and features overlapping with Rubinstein-Taybi syndrome. Czeschik JC; Albrecht B; Kayserili H; Kuechler A; Wagner N; Wieczorek D; Lüdecke HJ Clin Dysmorphol; 2014 Apr; 23(2):67-70. PubMed ID: 24561647 [No Abstract] [Full Text] [Related]
45. Confirmation of assignment of a locus for Rubinstein-Taybi syndrome gene to 16p13.3. Lacombe D; Saura R; Taine L; Battin J Am J Med Genet; 1992 Sep; 44(1):126-8. PubMed ID: 1519642 [TBL] [Abstract][Full Text] [Related]
47. [Goniodysgenesis associated with Rubinstein-Taybi syndrome]. Wajda M; Turno-Krecicka A Klin Oczna; 2000; 102(2):139-41. PubMed ID: 10932897 [TBL] [Abstract][Full Text] [Related]
48. Medical applications of dermatoglyphics. Schaumann B; Johnson SB Prog Clin Biol Res; 1982; 84():33-44. PubMed ID: 7100197 [No Abstract] [Full Text] [Related]
49. Cryptic microdeletion of the CREBBP gene from t(1;16) (p36.2;p13.3) as a novel genetic defect causing Rubinstein-Taybi syndrome. Kim SR; Kim HJ; Kim YJ; Kwon JY; Kim JW; Kim SH Ann Clin Lab Sci; 2013; 43(4):450-6. PubMed ID: 24247805 [TBL] [Abstract][Full Text] [Related]
54. From Whole Gene Deletion to Point Mutations of EP300-Positive Rubinstein-Taybi Patients: New Insights into the Mutational Spectrum and Peculiar Clinical Hallmarks. Negri G; Magini P; Milani D; Colapietro P; Rusconi D; Scarano E; Bonati MT; Priolo M; Crippa M; Mazzanti L; Wischmeijer A; Tamburrino F; Pippucci T; Finelli P; Larizza L; Gervasini C Hum Mutat; 2016 Feb; 37(2):175-83. PubMed ID: 26486927 [TBL] [Abstract][Full Text] [Related]
55. Rubinstein-Taybi syndrome caused by submicroscopic deletions within 16p13.3. Breuning MH; Dauwerse HG; Fugazza G; Saris JJ; Spruit L; Wijnen H; Tommerup N; van der Hagen CB; Imaizumi K; Kuroki Y; van den Boogaard MJ; de Pater JM; Mariman EC; Hamel BC; Himmelbauer H; Frischauf AM; Stallings R; Beverstock GC; van Ommen GJ; Hennekam RC Am J Hum Genet; 1993 Feb; 52(2):249-54. PubMed ID: 8430691 [TBL] [Abstract][Full Text] [Related]
56. [Rubinstein-Taybi syndrome in 4 cases]. Labenne M; Noir A; Amsallem D; Bertrand AM; Menget A; Burguet A Pediatrie; 1990; 45(7-8):471-5. PubMed ID: 2170923 [TBL] [Abstract][Full Text] [Related]
57. Submicroscopic deletions at 16p13.3 in Rubinstein-Taybi syndrome: frequency and clinical manifestations in a North American population. Wallerstein R; Anderson CE; Hay B; Gupta P; Gibas L; Ansari K; Cowchock FS; Weinblatt V; Reid C; Levitas A; Jackson L J Med Genet; 1997 Mar; 34(3):203-6. PubMed ID: 9132490 [TBL] [Abstract][Full Text] [Related]
58. Paraovarian Cyst Torsion in a Patient with Rubinstein-Taybi Syndrome: A Case Report. Kuwabara J; Akita S; Sato M; Watanabe K; Tanigawa K; Matsuno Y; Abe Y; Kikuchi S; Yoshida M; Koga S; Ishimaru K; Watanabe Y J Nippon Med Sch; 2021 Jun; 88(3):248-252. PubMed ID: 32863342 [TBL] [Abstract][Full Text] [Related]
59. Oral and dental manifestations in Rubinstein-Taybi syndrome: report of a rare case. Gunashekhar M; Hameed MS; Bokhari SK Prim Dent Care; 2012 Jan; 19(1):35-8. PubMed ID: 22244492 [TBL] [Abstract][Full Text] [Related]