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Journal Abstract Search
187 related items for PubMed ID: 10671068
1. Twelve novel RB1 gene mutations in patients with hereditary retinoblastoma. Mutations in brief no. 206. Online. Yilmaz S, Horsthemke B, Lohmann DR. Hum Mutat; 1998; 12(6):434. PubMed ID: 10671068 [Abstract] [Full Text] [Related]
2. Identification of 26 new constitutional RB1 gene mutations in Spanish, Colombian, and Cuban retinoblastoma patients. Alonso J, Frayle H, Menéndez I, López A, García-Miguel P, Abelairas J, Sarret E, Vendrell MT, Navajas A, Artigas M, Indiano JM, Carbone A, Torrenteras C, Palacios I, Pestaña A. Hum Mutat; 2005 Jan; 25(1):99. PubMed ID: 15605413 [Abstract] [Full Text] [Related]
5. Novel RB1 gene constitutional mutations found in Polish patients with familial and/or bilateral retinoblastoma. Jakubowska A, Zajaczek S, Haus O, Limon J, Kostyk E, Krzystolik Z, Lubinski J. Hum Mutat; 2001 Nov; 18(5):459. PubMed ID: 11668642 [Abstract] [Full Text] [Related]
6. Detection of mosaic RB1 mutations in families with retinoblastoma. Rushlow D, Piovesan B, Zhang K, Prigoda-Lee NL, Marchong MN, Clark RD, Gallie BL. Hum Mutat; 2009 May; 30(5):842-51. PubMed ID: 19280657 [Abstract] [Full Text] [Related]
7. Attenuation of disease phenotype through alternative translation initiation in low-penetrance retinoblastoma. Sánchez-Sánchez F, Ramírez-Castillejo C, Weekes DB, Beneyto M, Prieto F, Nájera C, Mittnacht S. Hum Mutat; 2007 Feb; 28(2):159-67. PubMed ID: 16988938 [Abstract] [Full Text] [Related]
15. Spectrum of gross deletions and insertions in the RB1 gene in patients with retinoblastoma and association with phenotypic expression. Albrecht P, Ansperger-Rescher B, Schüler A, Zeschnigk M, Gallie B, Lohmann DR. Hum Mutat; 2005 Nov; 26(5):437-45. PubMed ID: 16127685 [Abstract] [Full Text] [Related]
16. Loss of heterozygosity and mutations are the major mechanisms of RB1 gene inactivation in Chinese with sporadic retinoblastoma. Choy KW, Pang CP, Yu CB, Wong HL, Ng JS, Fan DS, Lo KW, Chai JT, Wang J, Fu W, Lam DS. Hum Mutat; 2002 Nov; 20(5):408. PubMed ID: 12402348 [Abstract] [Full Text] [Related]