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4. A new case of Myhre syndrome. Whiteford ML; Doig WB; Raine PA; Hollman AS; Tolmie JL Clin Dysmorphol; 2001 Apr; 10(2):135-40. PubMed ID: 11310994 [TBL] [Abstract][Full Text] [Related]
5. Rubinstein-Taybi syndrome. Berry AC J Med Genet; 1987 Sep; 24(9):562-6. PubMed ID: 3312608 [No Abstract] [Full Text] [Related]
6. Dominant inheritance of a syndrome similar to Rubinstein-Taybi. Cotsirilos P; Taylor JC; Matalon R Am J Med Genet; 1987 Jan; 26(1):85-93. PubMed ID: 3812583 [TBL] [Abstract][Full Text] [Related]
7. Rubinstein-Taybi syndrome. Review of 732 cases and analysis of the typical traits. Cantani A; Gagliesi D Eur Rev Med Pharmacol Sci; 1998; 2(2):81-7. PubMed ID: 10229563 [TBL] [Abstract][Full Text] [Related]
8. Rubinstein-Taybi syndrome: further evidence of a genetic aetiology. Gillies DR; Roussounis SH Dev Med Child Neurol; 1985 Dec; 27(6):751-5. PubMed ID: 4092848 [TBL] [Abstract][Full Text] [Related]
9. A patient with 9q subtelomeric deletion syndrome with additional findings. Tug E; Cavdarli B; Karaoguz MY; Percin FE Genet Couns; 2012; 23(4):465-71. PubMed ID: 23431745 [TBL] [Abstract][Full Text] [Related]
10. Rubinstein-Taybi syndrome in an oriental boy. Yang K; Yuh YS; Ch'ien LT Ala J Med Sci; 1982 Jan; 19(1):19-21. PubMed ID: 7059004 [No Abstract] [Full Text] [Related]
11. Rubinstein-Taybi syndrome: report of a case in a Nigerian child. Okoroma EO; Izuora GI J Natl Med Assoc; 1987 Nov; 79(11):1198-200. PubMed ID: 3694698 [TBL] [Abstract][Full Text] [Related]
12. Rubinstein-Taybi syndrome associated with Dandy-Walker cyst. Case report in a newborn. Mazzone D; Milana A; Praticò G; Reitano G J Perinat Med; 1989; 17(5):381-4. PubMed ID: 2625658 [TBL] [Abstract][Full Text] [Related]
13. [Rubinstein-Taybi syndrome. (2 cases studied also from a chromosomal point of view)]. Giovannucci ML; Calabri G Haematologica; 1969; 54(12):899-919. PubMed ID: 4993256 [No Abstract] [Full Text] [Related]
15. Cardiac abnormalities in the Rubinstein-Taybi syndrome. Stevens CA; Bhakta MG Am J Med Genet; 1995 Nov; 59(3):346-8. PubMed ID: 8599359 [TBL] [Abstract][Full Text] [Related]
16. Leukemia in Cardio-facio-cutaneous (CFC) syndrome: a patient with a germline mutation in BRAF proto-oncogene. Makita Y; Narumi Y; Yoshida M; Niihori T; Kure S; Fujieda K; Matsubara Y; Aoki Y J Pediatr Hematol Oncol; 2007 May; 29(5):287-90. PubMed ID: 17483702 [TBL] [Abstract][Full Text] [Related]
17. Epigenetic factors in intellectual disability: the Rubinstein-Taybi syndrome as a paradigm of neurodevelopmental disorder with epigenetic origin. Lopez-Atalaya JP; Valor LM; Barco A Prog Mol Biol Transl Sci; 2014; 128():139-76. PubMed ID: 25410544 [TBL] [Abstract][Full Text] [Related]
18. [Syndrome of congenital facial and finger anomalies associated with mental deficiency in an infant (Rubinstein-Taybi syndrome)]. Krauze M; Waclawczyk H; Marek J; Swiszcz A; Stoińska H Pol Tyg Lek; 1973 Dec; 28(49):1947-9. PubMed ID: 4770486 [No Abstract] [Full Text] [Related]