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216 related items for PubMed ID: 8926652
1. Mutation detection and genetic counseling in retinoblastoma using heteroduplex analysis. Zhang Q, Minoda K. Jpn J Ophthalmol; 1995; 39(4):432-7. PubMed ID: 8926652 [Abstract] [Full Text] [Related]
2. Detection of heterozygous mutations in the RB1 gene in retinoblastoma patients using single-strand conformation polymorphism analysis and polymerase chain reaction sequencing. Hogg A, Onadim Z, Baird PN, Cowell JK. Oncogene; 1992 Jul; 7(7):1445-51. PubMed ID: 1352398 [Abstract] [Full Text] [Related]
3. [Genetics of retinoblastoma]. Minoda K. Nihon Rinsho; 1995 Nov; 53(11):2774-8. PubMed ID: 8538043 [Abstract] [Full Text] [Related]
4. Mutations in the retinoblastoma gene and their expression in somatic and tumor cells of patients with hereditary retinoblastoma. Kato MV, Ishizaki K, Toguchida J, Kaneko A, Takayama J, Tanooka H, Kato T, Shimizu T, Sasaki MS. Hum Mutat; 1994 Nov; 3(1):44-51. PubMed ID: 8118465 [Abstract] [Full Text] [Related]
5. Independent constitutional germline mutations occurring in the RB1 gene in cousins with bilateral retinoblastoma. Bia B, Cowell JK. Oncogene; 1995 Sep 07; 11(5):977-9. PubMed ID: 7675457 [Abstract] [Full Text] [Related]
6. A familial RB1 mutation detected by the HOT technique is homozygous in a second primary neoplasm. Weir-Thompson E, Condie A, Leonard RC, Prosser J. Oncogene; 1991 Dec 07; 6(12):2353-6. PubMed ID: 1662795 [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 07; 28(2):159-67. PubMed ID: 16988938 [Abstract] [Full Text] [Related]
8. Spectrum of germline RB1 gene mutations in Spanish retinoblastoma patients: Phenotypic and molecular epidemiological implications. Alonso J, García-Miguel P, Abelairas J, Mendiola M, Sarret E, Vendrell MT, Navajas A, Pestaña A. Hum Mutat; 2001 May 07; 17(5):412-22. PubMed ID: 11317357 [Abstract] [Full Text] [Related]
9. [VNTR-PCR in diagnosis of inherited Rb gene mutation]. Zajaczek S, Górski B, Débniak T, Podolski J, Lubiński J, Krzystolik Z, Iwanicka T, Sagan Z. Klin Oczna; 1994 May 07; 96(8-9):290-2. PubMed ID: 7897998 [Abstract] [Full Text] [Related]
10. Identification of three new mutations in the RB1 gene in patients with sporadic retinoblastoma in Colombia. Serrano ML, Yunis JJ. Biomedica; 2013 May 07; 33(1):53-61. PubMed ID: 23715307 [Abstract] [Full Text] [Related]
11. [Low-penetrance retinoblastoma due to exons 24 and 25 deletions in the Rb1 gene]. Du C, Jiang Y, Gallie BL. Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2002 Oct 07; 19(5):370-4. PubMed ID: 12362308 [Abstract] [Full Text] [Related]
17. Unilateral retinoblastoma, lack of familial history and older age does not exclude germline RB1 gene mutation. Brichard B, Heusterspreute M, De Potter P, Chantrain C, Vermylen C, Sibille C, Gala JL. Eur J Cancer; 2006 Jan 07; 42(1):65-72. PubMed ID: 16343894 [Abstract] [Full Text] [Related]
18. Sensitive multistep clinical molecular screening of 180 unrelated individuals with retinoblastoma detects 36 novel mutations in the RB1 gene. Nichols KE, Houseknecht MD, Godmilow L, Bunin G, Shields C, Meadows A, Ganguly A. Hum Mutat; 2005 Jun 07; 25(6):566-74. PubMed ID: 15884040 [Abstract] [Full Text] [Related]