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3. Single cell detection of inherited retinoblastoma predisposition. Sütterlin M; Sleiman PA; Onadim Z; Delhanty J Prenat Diagn; 1999 Dec; 19(13):1231-6. PubMed ID: 10660960 [TBL] [Abstract][Full Text] [Related]
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5. A Dde I RFLP in exon 21 of human EL1 gene, encoding protein 4.1, detectable by SSCP. Maillet P; Dalla Venezia N; Bozon M; Vallier A; Delaunay J; Baklouti F Hum Mutat; 1998; 11(4):342-3. PubMed ID: 9554757 [TBL] [Abstract][Full Text] [Related]
6. [Diagnosis of a predisposition of retinoblastoma at the DNA level]. Murakami Y Gan To Kagaku Ryoho; 1991 Jan; 18(1):44-50. PubMed ID: 1670986 [TBL] [Abstract][Full Text] [Related]
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8. Utilization of a polymorphic variable-number-tandem-repeat DNA region within the RB1 gene for early diagnosis of hereditary retinoblastoma. Herzog R; Ben Arush MW; Ezer S; On MG; Lev Z Isr J Med Sci; 1993 May; 29(5):312-3. PubMed ID: 8100222 [No Abstract] [Full Text] [Related]
9. Low frequency of oncogenic mutations in the core promoter region of the RB1 gene. Fujita T; Ohtani-Fujita N; Sakai T; Rapaport JM; Dryja TP; Kato MV; Ishizaki K; Sasaki MS; Hotta Y; Maeda K; Kinoshita S; Ohnishi Y; Minoda K Hum Mutat; 1999; 13(5):410-1. PubMed ID: 10338096 [No Abstract] [Full Text] [Related]
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11. Identification of four novel RB1 germline mutations in Korean retinoblastoma patients. Yu YS; Kim IJ; Ku JL; Park JG Hum Mutat; 2001 Sep; 18(3):252. PubMed ID: 11524739 [TBL] [Abstract][Full Text] [Related]
12. Multiple lipomas linked to an RB1 gene mutation in a large pedigree with low penetrance retinoblastoma. Genuardi M; Klutz M; Devriendt K; Caruso D; Stirpe M; Lohmann DR Eur J Hum Genet; 2001 Sep; 9(9):690-4. PubMed ID: 11571558 [TBL] [Abstract][Full Text] [Related]
13. DNA fingerprints of Trichinella as revealed by restriction fragment length polymorphism and single-strand conformational polymorphism (RFLP-SSCP). Wu Z; Nakada T; Nagano I; Takahashi Y Mol Cell Probes; 2000 Oct; 14(5):291-7. PubMed ID: 11040092 [TBL] [Abstract][Full Text] [Related]
14. Systematic screening of type B human natriuretic peptide receptor gene polymorphisms and association with essential hypertension. Rahmutula D; Nakayama T; Soma M; Sato M; Izumi Y; Kanmatsuse K; Ozawa Y J Hum Hypertens; 2001 Jul; 15(7):471-4. PubMed ID: 11464256 [TBL] [Abstract][Full Text] [Related]
15. Two independent RB1-inactivating mutations in peripheral blood DNA of a hereditary retinoblastoma patient. Alonso J; Menéndez I; López A; Frayle H; Ruisánchez N; Pestaña A Genes Chromosomes Cancer; 2004 Jul; 40(3):271-5. PubMed ID: 15139006 [TBL] [Abstract][Full Text] [Related]
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19. [RFLP-PCR technique for exclusion of carrier status of the mutated Rb gene]. Zajaczek S; Podolski J; Lubiński J; Rosławska A; Krzystolik Z; Sagan Z Klin Oczna; 1993 Jun; 95(6):216-8. PubMed ID: 7905940 [TBL] [Abstract][Full Text] [Related]
20. [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; 19(5):370-4. PubMed ID: 12362308 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]