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534 related items for PubMed ID: 27436784
1. Epigenotype, genotype, and phenotype analysis of patients in Taiwan with Beckwith-Wiedemann syndrome. Lin HY, Chuang CK, Tu RY, Fang YY, Su YN, Chen CP, Chang CY, Liu HC, Chu TH, Niu DM, Lin SP. Mol Genet Metab; 2016 Sep; 119(1-2):8-13. PubMed ID: 27436784 [Abstract] [Full Text] [Related]
2. (Epi)genotype-phenotype correlations in Beckwith-Wiedemann syndrome. Mussa A, Russo S, De Crescenzo A, Freschi A, Calzari L, Maitz S, Macchiaiolo M, Molinatto C, Baldassarre G, Mariani M, Tarani L, Bedeschi MF, Milani D, Melis D, Bartuli A, Cubellis MV, Selicorni A, Cirillo Silengo M, Larizza L, Riccio A, Ferrero GB. Eur J Hum Genet; 2016 Feb; 24(2):183-90. PubMed ID: 25898929 [Abstract] [Full Text] [Related]
3. Investigation of (epi)genotype causes and follow-up manifestations in the patients with classical and atypical phenotype of Beckwith-Wiedemann spectrum. Tüysüz B, Güneş N, Geyik F, Yeşil G, Celkan T, Vural M. Am J Med Genet A; 2021 Jun; 185(6):1721-1731. PubMed ID: 33704912 [Abstract] [Full Text] [Related]
4. Epigenotype and phenotype correlations in patients with Beckwith-Wiedemann syndrome. Bilgin B, Kabaçam S, Taşkıran E, Şimşek-Kiper PÖ, Alanay Y, Boduroğlu K, Utine GE. Turk J Pediatr; 2018 Jun; 60(5):506-513. PubMed ID: 30968633 [Abstract] [Full Text] [Related]
14. Clinical and molecular features of children with Beckwith-Wiedemann syndrome in China: a single-center retrospective cohort study. Wang R, Xiao Y, Li D, Hu H, Li X, Ge T, Yu R, Wang Y, Zhang T. Ital J Pediatr; 2020 Apr 29; 46(1):55. PubMed ID: 32349794 [Abstract] [Full Text] [Related]
15. Epigenotype-phenotype correlations in Beckwith-Wiedemann syndrome. Engel JR, Smallwood A, Harper A, Higgins MJ, Oshimura M, Reik W, Schofield PN, Maher ER. J Med Genet; 2000 Dec 29; 37(12):921-6. PubMed ID: 11106355 [Abstract] [Full Text] [Related]
16. Deciphering Epigenetic Backgrounds in a Korean Cohort with Beckwith-Wiedemann Syndrome. Kim HY, Shin CH, Lee YA, Shin CH, Kim GH, Ko JM. Ann Lab Med; 2022 Nov 01; 42(6):668-677. PubMed ID: 35765875 [Abstract] [Full Text] [Related]