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Journal Abstract Search

142 related items for PubMed ID: 2570677

  • 1. 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; 50(2-3):70-4. PubMed ID: 2570677
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  • 2. 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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  • 3. The beta-subunit of follicle-stimulating hormone is deleted in patients with aniridia and Wilms' tumour, allowing a further definition of the WAGR locus.
    Glaser T, Lewis WH, Bruns GA, Watkins PC, Rogler CE, Shows TB, Powers VE, Willard HF, Goguen JM, Simola KO.
    Nature; 1988 Aug; 321(6073):882-7. PubMed ID: 3014343
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  • 4. 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 Aug; 66(2-3):181-5. PubMed ID: 6325323
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  • 6. Two anonymous DNA segments distinguish the Wilms' tumor and aniridia loci.
    Davis LM, Stallard R, Thomas GH, Couillin P, Junien C, Nowak NJ, Shows TB.
    Science; 1988 Aug 12; 241(4867):840-2. PubMed ID: 2841760
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  • 10. Rapid isolation of moderate and highly polymorphic DNA fragments mapping close to WT (Wilms' tumour) and AN2 (aniridia) on chromosome 11.
    Boyd PA, Christie S, Hastie ND, Porteous DJ.
    Hum Genet; 1989 Mar 12; 81(4):349-52. PubMed ID: 2564837
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  • 11. Aniridia, Wilms' tumor and human chromosome 11.
    Bickmore WA, Hastie ND.
    Ophthalmic Paediatr Genet; 1989 Dec 12; 10(4):229-48. PubMed ID: 2560823
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  • 14. Pericentric intrachromosomal insertion responsible for recurrence of del(11)(p13p14) in a family.
    Henry I, Hoovers J, Barichard F, Berthéas MF, Puech A, Prieur F, Gessler M, Bruns G, Mannens M, Junien C.
    Genes Chromosomes Cancer; 1993 May 12; 7(1):57-62. PubMed ID: 7688557
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  • 16. Familial occurrence of the aniridia-Wilms tumor syndrome with deletion 11p13-14.1.
    Yunis JJ, Ramsay NK.
    J Pediatr; 1980 Jun 12; 96(6):1027-30. PubMed ID: 6246230
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  • 17. 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 12; 11(2):284-93. PubMed ID: 1769647
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