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Journal Abstract Search

118 related items for PubMed ID: 8004094

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  • 5. Three Finnish incontinentia pigmenti (IP) families with recombinations with the IP loci at Xq28 and Xp11.
    Hydén-Granskog C, Salonen R, von Koskull H.
    Hum Genet; 1993 Mar; 91(2):185-9. PubMed ID: 8096494
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  • 6. The gene for incontinentia pigmenti is assigned to Xq28.
    Sefiani A, Abel L, Heuertz S, Sinnett D, Lavergne L, Labuda D, Hors-Cayla MC.
    Genomics; 1989 Apr; 4(3):427-9. PubMed ID: 2714798
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  • 7. Transcriptional analysis of the candidate region for incontinentia pigmenti (IP2) in Xq28.
    Rogner UC, Heiss NS, Kioschis P, Wiemann S, Korn B, Poustka A.
    Genome Res; 1996 Oct; 6(10):922-34. PubMed ID: 8908511
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  • 8. The gene for X-linked hydrocephalus maps to Xq28, distal to DXS52.
    Lyonnet S, Pelet A, Royer G, Delrieu O, Serville F, le Marec B, Gruensteudel A, Pfeiffer RA, Briard ML, Dubay C.
    Genomics; 1992 Oct; 14(2):508-10. PubMed ID: 1427869
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  • 13. De Novo incontinentia pigmenti in female twins.
    Su PH, Chen JY, Yu JS, Su CM, Huang TC, Chen SJ.
    Acta Paediatr Taiwan; 2004 Oct; 45(3):178-80. PubMed ID: 15493740
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  • 14. Selection against mutant alleles in blood leukocytes is a consistent feature in Incontinentia Pigmenti type 2.
    Parrish JE, Scheuerle AE, Lewis RA, Levy ML, Nelson DL.
    Hum Mol Genet; 1996 Nov; 5(11):1777-83. PubMed ID: 8923006
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  • 15. Recent progress in the genetics of incontinentia pigmenti (Bloch-Sulzberger syndrome).
    Shastry BS.
    J Hum Genet; 2000 Nov; 45(6):323-6. PubMed ID: 11185738
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  • 17. Mapping to distal Xq28 of nonspecific X-linked mental retardation MRX72: linkage analysis and clinical findings in a three-generation Sardinian family.
    Russo S, Cogliati F, Cavalleri F, Cassitto MG, Giglioli R, Toniolo D, Casari G, Larizza L.
    Am J Med Genet; 2000 Oct 23; 94(5):376-82. PubMed ID: 11050621
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  • 19. Further localization of X-linked hydrocephalus in the chromosomal region Xq28.
    Willems PJ, Vits L, Raeymaekers P, Beuten J, Coucke P, Holden JJ, Van Broeckhoven C, Warren ST, Sagi M, Robinson D.
    Am J Hum Genet; 1992 Aug 23; 51(2):307-15. PubMed ID: 1642232
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