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Journal Abstract Search

139 related items for PubMed ID: 1849870

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  • 25. 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; 66(2-3):181-5. PubMed ID: 6325323
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  • 26. Aniridia--Wilms' tumour association--a case with 11p 13-14.1 deletion and ventricular septal defect.
    Rao SR, Athale UH, Kadam PR, Gladstone B, Nair CN, Pai SK, Kurkure PA, Advani SH.
    Indian J Cancer; 1992 Sep; 29(3):117-21. PubMed ID: 1338056
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  • 30. Constitutional mutations in the WT1 gene in patients with Denys-Drash syndrome.
    Baird PN, Santos A, Groves N, Jadresic L, Cowell JK.
    Hum Mol Genet; 1992 Aug; 1(5):301-5. PubMed ID: 1338906
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  • 32. Familial occurrence of the aniridia-Wilms tumor syndrome with deletion 11p13-14.1.
    Yunis JJ, Ramsay NK.
    J Pediatr; 1980 Jun; 96(6):1027-30. PubMed ID: 6246230
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  • 35. Polymerase chain reaction-based risk assessment for Wilms tumor in sporadic aniridia.
    Gupta SK, De Becker I, Guernsey DL, Neumann PE.
    Am J Ophthalmol; 1998 May; 125(5):687-92. PubMed ID: 9625553
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  • 37. Molecular definition of de novo and genetically transmitted WAGR-associated rearrangements of 11p13.
    Lavedan C, Barichard F, Azoulay M, Couillin P, Molina Gomez D, Nicolas H, Quack B, Rethoré MO, Noel B, Junien C.
    Cytogenet Cell Genet; 1989 May; 50(2-3):70-4. PubMed ID: 2570677
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  • 38. 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; 3(2):117-23. PubMed ID: 2852160
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  • 39. 11p13 deletion, Wilms' tumour, and aniridia: unusual genetic, non-ocular and ocular features of three cases.
    Jotterand V, Boisjoly HM, Harnois C, Bigonesse P, Laframboise R, Gagné R, St-Pierre A.
    Br J Ophthalmol; 1990 Sep; 74(9):568-70. PubMed ID: 2168204
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