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Journal Abstract Search

94 related items for PubMed ID: 1362326

  • 1. Prenatal exclusion of choroideremia.
    van den Hurk JA, van Zandvoort PM, Brunsmann F, Pawlowitzki IH, Holzgreve W, Szabo P, Cremers FP, van Oost BA.
    Am J Med Genet; 1992 Dec 01; 44(6):822-3. PubMed ID: 1362326
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  • 3. Identification of mutations in Danish choroideremia families.
    Schwartz M, Rosenberg T, van den Hurk JA, van de Pol DJ, Cremers FP.
    Hum Mutat; 1993 Dec 01; 2(1):43-7. PubMed ID: 8477262
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  • 5. First-trimester prenatal molecular diagnosis of infantile hypophosphatasia in a Japanese family.
    Orimo H, Nakajima E, Hayashi Z, Kijima K, Watanabe A, Tenjin H, Araki T, Shimada T.
    Prenat Diagn; 1996 Jun 01; 16(6):559-63. PubMed ID: 8809899
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  • 9. An exonic polymorphism (381A/G) in the choroideremia gene.
    Beaufrere L, Tuffery S, Hamel C, Bareil C, Arnaud B, Demaille J, Claustres M.
    Genet Couns; 1997 Jun 01; 8(3):223-5. PubMed ID: 9327266
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  • 13. Prenatal diagnosis of carnitine palmitoyltransferase 2 deficiency in chorionic villi: a novel approach.
    Vekemans BC, Bonnefont JP, Aupetit J, Royer G, Droin V, Attié-Bitach T, Saudubray JM, Thuillier L.
    Prenat Diagn; 2003 Nov 01; 23(11):884-7. PubMed ID: 14634971
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  • 16. [Presymptomatic DNA diagnosis in Huntington chorea with linked DNA markers].
    Thies U, Schröder K, Bockel B, Zoll B, Lange H.
    Nervenarzt; 1991 Oct 01; 62(10):615-20. PubMed ID: 1684226
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  • 17. A rapid PCR-based method to distinguish between fetal and maternal cells in chorionic biopsies using microsatellite polymorphisms.
    Noble JS, Taylor GR, Stewart AD, Mueller RF, Murday VA.
    Dis Markers; 1991 Oct 01; 9(6):301-6. PubMed ID: 1823308
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  • 18. Prenatal diagnosis of choroideremia.
    Schwartz M, Rosenberg T.
    Acta Ophthalmol Scand Suppl; 1996 Oct 01; (219):33-6. PubMed ID: 8741114
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  • 19. Prenatal diagnosis of alpha-1-antitrypsin deficiency using polymerase chain reaction (PCR). Comparison of conventional RFLP methods with PCR used in combination with allele specific oligonucleotides or RFLP analysis.
    Schwartz M, Petersen KB, Gregersen N, Hinkel K, Newton CR.
    Clin Genet; 1989 Dec 01; 36(6):419-26. PubMed ID: 2574085
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