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144 related items for PubMed ID: 1390533

  • 1. Prenatal exclusion of Norrie's disease.
    Redmond RM, Graham CA, Kelly ED, Coleman M, Nevin NC.
    Br J Ophthalmol; 1992 Aug; 76(8):491-3. PubMed ID: 1390533
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  • 4. Probably Norrie's disease due to mutation. Two sporadic sibships of two males each, a necropsy of one case, and, given Norrie's disease, a calculation of the gene mutation frequency.
    Phillips CI, Newton M, Duvall J, Holloway S, Levy AM.
    Br J Ophthalmol; 1986 Apr; 70(4):305-13. PubMed ID: 3964631
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  • 5. Norrie's disease: delineation of carriers among daughters of obligate carriers by linkage analysis.
    Warburg M, Friedrich U, Bleeker-Wagemakers L, Wienker TF, Gal A, Ropers HH.
    Trans Ophthalmol Soc U K (1962); 1986 Apr; 105 ( Pt 1)():88-93. PubMed ID: 3459299
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  • 7. Carrier detection and prenatal diagnosis in Norrie disease.
    Curtis D, Blank CE, Parsons MA, Hughes HN.
    Prenat Diagn; 1989 Oct; 9(10):735-40. PubMed ID: 2574445
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  • 8. Prenatal diagnosis of X-linked retinitis pigmentosa (RP) in five pregnancies at risk.
    Iampieri MP, Mingarelli R, Le Guern E, Novelli G, Dallapiccola B.
    Prenat Diagn; 1994 Apr; 14(4):285-9. PubMed ID: 8066038
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  • 9. Manifesting heterozygosity in Norrie's disease?
    Woodruff G, Newbury-Ecob R, Plaha DS, Young ID.
    Br J Ophthalmol; 1993 Dec; 77(12):813-4. PubMed ID: 8110678
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  • 10. Norrie's disease: close linkage with genetic markers from the proximal short arm of the X chromosome.
    Gal A, Stolzenberger C, Wienker T, Wieacker P, Ropers HH, Friedrich U, Bleeker-Wagemakers L, Pearson P, Warburg M.
    Clin Genet; 1985 Mar; 27(3):282-3. PubMed ID: 3857130
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  • 11. Prenatal exclusion of X-linked hydrocephalus-stenosis of the aqueduct of Sylvius sequence using closely linked DNA markers.
    Serville F, Benit P, Saugier P, Vibert M, Royer G, Pelet A, Chery M, Munnich A, Lyonnet S.
    Prenat Diagn; 1993 Jun; 13(6):435-9. PubMed ID: 8372068
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  • 12. Prenatal exclusion of Norrie disease with flanking DNA markers.
    Gal A, Uhlhaas S, Glaser D, Grimm T.
    Am J Med Genet; 1988 Oct; 31(2):449-53. PubMed ID: 3068991
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  • 13. Prenatal diagnosis of adult polycystic kidney disease with DNA markers on chromosome 16 and the genetic heterogeneity problem.
    Novelli G, Frontali M, Baldini D, Bosman C, Dallapiccola B, Pachì A, Torcia F.
    Prenat Diagn; 1989 Nov; 9(11):759-67. PubMed ID: 2616535
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  • 14. Restriction enzyme analysis of Norrie disease pedigrees.
    Chung SR, Katayama S, Lebo R, Golbus MS.
    Asia Oceania J Obstet Gynaecol; 1992 Sep; 18(3):255-61. PubMed ID: 1360203
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  • 15. Secrets of life in a spoonful of blood.
    Ainsworth C.
    Nature; 2017 Feb 07; 542(7640):156-158. PubMed ID: 28179684
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  • 16. Norrie's disease in a French-Canadian kindred: attempt to detect carriers by DNA analysis.
    Polomeno RC, Zeesman S, MacDonald IM, Crozier DG, Tenniswood MP, Kaplan P.
    Can J Ophthalmol; 1987 Feb 07; 22(1):21-3. PubMed ID: 3815151
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  • 17. [Prenatal diagnosis for fetus with hemophilia A].
    Zhao Y, Liang Y, Wang ZY, Xiao B.
    Zhonghua Fu Chan Ke Za Zhi; 2008 Apr 07; 43(4):262-5. PubMed ID: 18843965
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  • 18. The molecular biology of Norrie's disease.
    Black G, Redmond RM.
    Eye (Lond); 1994 Apr 07; 8 ( Pt 5)():491-6. PubMed ID: 7835440
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  • 19. Prenatal diagnosis of cystic fibrosis.
    Christian CL.
    Clin Perinatol; 1990 Dec 07; 17(4):779-91. PubMed ID: 2286028
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