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Journal Abstract Search

258 related items for PubMed ID: 7897998

  • 21. A novel mutation in the promotor region in a family with a mild form of retinoblastoma indicates the location of a new regulatory domain for the RB1 gene.
    Cowell JK, Bia B, Akoulitchev A.
    Oncogene; 1996 Jan 18; 12(2):431-6. PubMed ID: 8570221
    [Abstract] [Full Text] [Related]

  • 22. [Mutations of several tumor suppressor genes in primary retinoblastoma].
    Huang Q, Tao Y, Yandell DW.
    Zhonghua Zhong Liu Za Zhi; 1999 Jan 18; 21(1):10-2. PubMed ID: 11776785
    [Abstract] [Full Text] [Related]

  • 23. Carrier detection by DNA linkage analysis in eighty Thai hemophilia A families.
    Mahasandana C, Pung-Amritt P, Treesucon A, Petrarat S, Veerakul G, Visudhiphan S, Yenchitsomanus PT.
    J Med Assoc Thai; 2002 Aug 18; 85 Suppl 2():S513-21. PubMed ID: 12403227
    [Abstract] [Full Text] [Related]

  • 24. Loss of heterozygosity in the VNTR region of intron 1 of P53 in two retinoblastoma cases.
    Emre S, Sungur A, Bilgiç S, Büyükpamukçu M, Günalp I, Ozgüç M.
    Pediatr Hematol Oncol; 1996 Aug 18; 13(3):253-6. PubMed ID: 8735341
    [Abstract] [Full Text] [Related]

  • 25. 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 18; 29(5):312-3. PubMed ID: 8100222
    [No Abstract] [Full Text] [Related]

  • 26. [Genetic counseling and interdisciplinary management of retinoblastoma].
    Müller H.
    Klin Monbl Augenheilkd; 1993 May 18; 202(5):433-6. PubMed ID: 8377409
    [Abstract] [Full Text] [Related]

  • 27. [Molecular diagnosis of Huntington's disease: an analysis of two large families].
    Zeng Y, Chen M, Mao Y.
    Zhonghua Yi Xue Za Zhi; 1995 Nov 18; 75(11):689-93, 711-2. PubMed ID: 8697093
    [Abstract] [Full Text] [Related]

  • 28. Oncogenic point mutations in the human retinoblastoma gene: their application to genetic counseling.
    Yandell DW, Campbell TA, Dayton SH, Petersen R, Walton D, Little JB, McConkie-Rosell A, Buckley EG, Dryja TP.
    N Engl J Med; 1989 Dec 21; 321(25):1689-95. PubMed ID: 2594029
    [Abstract] [Full Text] [Related]

  • 29. Hereditary retinoblastoma transmitted by maternal germline mosaicism.
    Barbosa RH, Vargas FR, Aguiar FC, Ferman S, Lucena E, Bonvicino CR, Seuánez HN.
    Pediatr Blood Cancer; 2008 Nov 21; 51(5):598-602. PubMed ID: 18661485
    [Abstract] [Full Text] [Related]

  • 30. [Simplified detection of RB gene mutation by PCR-SSCP method in human osteosarcoma].
    Isomi T.
    Nihon Seikeigeka Gakkai Zasshi; 1993 Nov 21; 67(11):1026-32. PubMed ID: 8283114
    [Abstract] [Full Text] [Related]

  • 31. [Spontaneous growth inhibition in retinoblastoma].
    Lommatzsch PK, Zimmermann W, Lommatzsch R.
    Klin Monbl Augenheilkd; 1993 Mar 21; 202(3):218-23. PubMed ID: 8510416
    [Abstract] [Full Text] [Related]

  • 32. [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 21; 19(5):370-4. PubMed ID: 12362308
    [Abstract] [Full Text] [Related]

  • 33. Detection of small RB1 gene deletions in retinoblastoma by multiplex PCR and high-resolution gel electrophoresis.
    Lohmann D, Horsthemke B, Gillessen-Kaesbach G, Stefani FH, Höfler H.
    Hum Genet; 1992 Apr 21; 89(1):49-53. PubMed ID: 1577465
    [Abstract] [Full Text] [Related]

  • 34. Deletion in one allele and a rare neutral DNA alteration in the other allele of the RB1 gene in a patient with bilateral retinoblastoma.
    Horsthemke B, Brandt B, Albrecht B, Passarge E.
    Am J Med Genet; 1992 Sep 15; 44(2):255. PubMed ID: 1456305
    [No Abstract] [Full Text] [Related]

  • 35. Effects of an Rb mutation in the mouse.
    Jacks T, Fazeli A, Schmitt EM, Bronson RT, Goodell MA, Weinberg RA.
    Nature; 1992 Sep 24; 359(6393):295-300. PubMed ID: 1406933
    [Abstract] [Full Text] [Related]

  • 36. Mutation spectrum of the retinoblastoma gene in osteosarcomas.
    Wadayama B, Toguchida J, Shimizu T, Ishizaki K, Sasaki MS, Kotoura Y, Yamamuro T.
    Cancer Res; 1994 Jun 01; 54(11):3042-8. PubMed ID: 8187094
    [Abstract] [Full Text] [Related]

  • 37. Retinoblastoma in India : microsatellite analysis and its application in genetic counseling.
    Ramprasad VL, Madhavan J, Murugan S, Sujatha J, Suresh S, Sharma T, Kumaramanickavel G.
    Mol Diagn Ther; 2007 Jun 01; 11(1):63-70. PubMed ID: 17286451
    [Abstract] [Full Text] [Related]

  • 38. Family studies in retinoblastoma.
    Gordon H.
    Birth Defects Orig Artic Ser; 1974 Jun 01; 10(10):185-90. PubMed ID: 4462631
    [No Abstract] [Full Text] [Related]

  • 39. [Carrier diagnosis of retinoblastoma with molecular genetic methods].
    Nordenskjöld M, Cavenee WK, Kumlin E, Kock E.
    Lakartidningen; 1984 Mar 21; 81(12):1183-92. PubMed ID: 6369047
    [No Abstract] [Full Text] [Related]

  • 40. Infrequent loss of heterozygosity of the major tumour suppressor genes in Indian oral cancers.
    Kannan S, Yokozaki H, Jayasree K, Sebastian P, Mathews A, Abraham EK, Nair MK, Tahara E.
    Int J Oral Maxillofac Surg; 2002 Aug 21; 31(4):414-8. PubMed ID: 12361076
    [Abstract] [Full Text] [Related]

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