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Journal Abstract Search

125 related items for PubMed ID: 7688557

  • 21. Molecular analysis of chromosome region 11p13 in patients with Drash syndrome.
    Jadresic L, Wadey RB, Buckle B, Barratt TM, Mitchell CD, Cowell JK.
    Hum Genet; 1991 Mar; 86(5):497-501. PubMed ID: 1849870
    [Abstract] [Full Text] [Related]

  • 22. A FISH approach to defining the extent and possible clinical significance of deletions at the WAGR locus.
    Crolla JA, Cawdery JE, Oley CA, Young ID, Gray J, Fantes J, van Heyningen V.
    J Med Genet; 1997 Mar; 34(3):207-12. PubMed ID: 9132491
    [Abstract] [Full Text] [Related]

  • 23. Four new DNA markers are assigned to the WAGR region of 11p13: isolation and regional assignment of 112 chromosome 11 anonymous DNA segments.
    Davis LM, Byers MG, Fukushima Y, Qin SZ, Nowak NJ, Scoggin C, Shows TB.
    Genomics; 1988 Oct; 3(3):264-71. PubMed ID: 2852164
    [Abstract] [Full Text] [Related]

  • 24. Chromosome number 11 and Wilms' tumor.
    Slater RM, de Kraker J.
    Cancer Genet Cytogenet; 1982 Mar; 5(3):237-45. PubMed ID: 6279277
    [Abstract] [Full Text] [Related]

  • 25. c-Ha-ras1 is not deleted in aniridia-Wilms' tumour association.
    Huerre C, Despoisse S, Gilgenkrantz S, Lenoir GM, Junien C.
    Nature; 1982 Mar; 305(5935):638-41. PubMed ID: 6312328
    [Abstract] [Full Text] [Related]

  • 26. Regional mapping of catalase and Wilms tumor--aniridia, genitourinary abnormalities, and mental retardation triad loci to the chromosome segment 11p1305----p1306.
    Narahara K, Kikkawa K, Kimira S, Kimoto H, Ogata M, Kasai R, Hamawaki M, Matsuoka K.
    Hum Genet; 1984 Mar; 66(2-3):181-5. PubMed ID: 6325323
    [Abstract] [Full Text] [Related]

  • 27. Submicroscopic deletions at the WAGR locus, revealed by nonradioactive in situ hybridization.
    Fantes JA, Bickmore WA, Fletcher JM, Ballesta F, Hanson IM, van Heyningen V.
    Am J Hum Genet; 1992 Dec; 51(6):1286-94. PubMed ID: 1334370
    [Abstract] [Full Text] [Related]

  • 28. [WAGR syndrome: a case report].
    Moreno García M, Sánchez del Pozo J, Fernández Martínez FJ, Moreno-Izquierdo A, Barreiro Miranda E.
    An Esp Pediatr; 1998 Oct; 49(4):381-7. PubMed ID: 9859552
    [Abstract] [Full Text] [Related]

  • 29. Altered trans-activational properties of a mutated WT1 gene product in a WAGR-associated Wilms' tumor.
    Park S, Tomlinson G, Nisen P, Haber DA.
    Cancer Res; 1993 Oct 15; 53(20):4757-60. PubMed ID: 8402654
    [Abstract] [Full Text] [Related]

  • 30. Analysis of WAGR deletions and related translocations with gene-specific DNA probes, using FACS-selected cell hybrids.
    Seawright A, Fletcher JM, Fantes JA, Morrison H, Porteous DJ, Li SS, Hastie ND, Van Heyningen V.
    Somat Cell Mol Genet; 1988 Jan 15; 14(1):21-30. PubMed ID: 2829363
    [Abstract] [Full Text] [Related]

  • 31. The gene for catalase is assigned between the antigen loci MIC4 and MIC11.
    Couillin P, Azoulay M, Metezeau P, Grisard MC, Junien C.
    Genomics; 1989 Jan 15; 4(1):7-11. PubMed ID: 2536636
    [Abstract] [Full Text] [Related]

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  • 33. Nonlinkage of 16q markers to familial predisposition to Wilms' tumor.
    Huff V, Reeve AE, Leppert M, Strong LC, Douglass EC, Geiser CF, Li FP, Meadows A, Callen DF, Lenoir G.
    Cancer Res; 1992 Nov 01; 52(21):6117-20. PubMed ID: 1356625
    [Abstract] [Full Text] [Related]

  • 34.
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  • 35. Molecular mapping and cloning of the breakpoints of a chromosome 11p14.1-p13 deletion associated with the AGR syndrome.
    Gessler M, Bruns GA.
    Genomics; 1988 Aug 01; 3(2):117-23. PubMed ID: 2852160
    [Abstract] [Full Text] [Related]

  • 36. The chromosome 11 region flanking the t(11;14) breakpoint in human T-ALL is deleted in Wilms' tumor hybrids.
    Finver SN, Martiniere C, Kagan J, Cavenee W, Croce CM.
    Oncogene Res; 1989 Aug 01; 5(2):143-8. PubMed ID: 2558334
    [Abstract] [Full Text] [Related]

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  • 38. The distal region of 11p13 and associated genetic diseases.
    Mannens M, Hoovers JM, Bleeker-Wagemakers EM, Redeker E, Bliek J, Overbeeke-Melkert M, Saunders G, Williams B, van Heyningen V, Junien C.
    Genomics; 1991 Oct 01; 11(2):284-93. PubMed ID: 1769647
    [Abstract] [Full Text] [Related]

  • 39. Loss of heterozygosity mapping in Wilms tumor indicates the involvement of three distinct regions and a limited role for nondisjunction or mitotic recombination.
    Coppes MJ, Bonetta L, Huang A, Hoban P, Chilton-MacNeill S, Campbell CE, Weksberg R, Yeger H, Reeve AE, Williams BR.
    Genes Chromosomes Cancer; 1992 Nov 01; 5(4):326-34. PubMed ID: 1283321
    [Abstract] [Full Text] [Related]

  • 40. Direct pulsed field gel electrophoresis of Wilms' tumors shows that DNA deletions in 11p13 are rare.
    Royer-Pokora B, Ragg S, Heckl-Ostreicher B, Held M, Loos U, Call K, Glaser T, Housman D, Saunders G, Zabel B.
    Genes Chromosomes Cancer; 1991 Mar 01; 3(2):89-100. PubMed ID: 1648959
    [Abstract] [Full Text] [Related]

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