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Journal Abstract Search

253 related items for PubMed ID: 6325323

  • 21.
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  • 23. High-resolution studies in patients with aniridia-Wilms tumor association, Wilms tumor or related congenital abnormalities.
    Nakagome Y, Ise T, Sakurai M, Nakajo T, Okamoto E, Takano T, Nakahori Y, Tsuchida Y, Nagahara N, Takada Y.
    Hum Genet; 1984; 67(3):245-8. PubMed ID: 6088386
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  • 26. Computer-assisted analysis of chromosomal abnormalities: detection of a deletion in aniridia-Wilms' tumor syndrome.
    Ladda R, Atkins L, Littlefield J, Neurath P, Marimuthu KM.
    Science; 1974 Aug 30; 185(4153):784-7. PubMed ID: 4367262
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  • 28. Familial occurrence of the aniridia-Wilms tumor syndrome with deletion 11p13-14.1.
    Yunis JJ, Ramsay NK.
    J Pediatr; 1980 Jun 30; 96(6):1027-30. PubMed ID: 6246230
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  • 29. Molecular analysis of gene deletion in aniridia--Wilms tumor association.
    Michalopoulos EE, Bevilacqua PJ, Stokoe N, Powers VE, Willard HF, Lewis WH.
    Hum Genet; 1985 Jun 30; 70(2):157-62. PubMed ID: 2989154
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  • 30. 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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  • 31. Molecular analysis of aniridia patients for deletions involving the Wilms' tumor gene.
    Drechsler M, Meijers-Heijboer EJ, Schneider S, Schurich B, Grond-Ginsbach C, Tariverdian G, Kantner G, Blankenagel A, Kaps D, Schroeder-Kurth T.
    Hum Genet; 1994 Oct 12; 94(4):331-8. PubMed ID: 7927324
    [Abstract] [Full Text] [Related]

  • 32. A highly polymorphic locus cloned from the breakpoint of a chromosome 11p13 deletion associated with the WAGR syndrome.
    Glaser T, Driscoll DJ, Antonarakis S, Valle D, Housman D.
    Genomics; 1989 Nov 12; 5(4):880-93. PubMed ID: 2574149
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  • 33. Wilms tumour: a developmental anomaly.
    Hastie ND, Bickmore W, Pritchard-Jones K, Porteous DJ, van Heyningen V.
    Princess Takamatsu Symp; 1989 Nov 12; 20():145-50. PubMed ID: 2562179
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  • 34.
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  • 35. WAGR(O?) syndrome and congenital ptosis caused by an unbalanced t(11;15)(p13;p11.2)dn demonstrating a 7 megabase deletion by FISH.
    Lennon PA, Scott DA, Lonsdorf D, Wargowski DS, Kirkpatrick S, Patel A, Cheung SW.
    Am J Med Genet A; 2006 Jun 01; 140(11):1214-8. PubMed ID: 16646034
    [Abstract] [Full Text] [Related]

  • 36. Wilms' tumor-aniridia association: segregation of affected chromosome in somatic cell hybrids, identification of cell surface antigen associated with deleted area, and regional mapping of c-Ha-ras-1 oncogene, insulin gene, and beta-globin gene.
    Fisher JH, Miller YE, Sparkes RS, Bateman JB, Kimmel KA, Carey TE, Rodell T, Shoemaker SA, Scoggin CH.
    Somat Cell Mol Genet; 1984 Sep 01; 10(5):455-64. PubMed ID: 6089356
    [Abstract] [Full Text] [Related]

  • 37. c-Ha-ras1 is not deleted in aniridia-Wilms' tumour association.
    Huerre C, Despoisse S, Gilgenkrantz S, Lenoir GM, Junien C.
    Nature; 1984 Sep 01; 305(5935):638-41. PubMed ID: 6312328
    [Abstract] [Full Text] [Related]

  • 38. 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 01; 3(3):264-71. PubMed ID: 2852164
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