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197 related items for PubMed ID: 9272741

  • 1. Linkage analysis in 16 families with incontinentia pigmenti.
    Jouet M, Stewart H, Landy S, Yates J, Yong SL, Harris A, Garret C, Hatchwell E, Read A, Donnai D, Kenwrick S.
    Eur J Hum Genet; 1997; 5(3):168-70. PubMed ID: 9272741
    [Abstract] [Full Text] [Related]

  • 2. 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
    [Abstract] [Full Text] [Related]

  • 3. 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
    [Abstract] [Full Text] [Related]

  • 4. Linkage relationship between incontinentia pigmenti (IP2) and nine terminal X long arm markers.
    Sefiani A, M'rad R, Simard L, Vincent A, Julier C, Holvoet-Vermaut L, Heuertz S, Dahl N, Stalder JF, Peter MO.
    Hum Genet; 1991 Jan; 86(3):297-9. PubMed ID: 1847690
    [Abstract] [Full Text] [Related]

  • 5. The gene for the familial form of incontinentia pigmenti (IP2) maps to the distal part of Xq28.
    Smahi A, Hyden-Granskog C, Peterlin B, Vabres P, Heuertz S, Fulchignoni-Lataud MC, Dahl N, Labrune P, Le Marec B, Piussan C.
    Hum Mol Genet; 1994 Feb; 3(2):273-8. PubMed ID: 8004094
    [Abstract] [Full Text] [Related]

  • 6. The molecular genetics of incontinentia pigmenti.
    Gorski JL, Burright EN.
    Semin Dermatol; 1993 Sep; 12(3):255-65. PubMed ID: 8105861
    [Abstract] [Full Text] [Related]

  • 7. A study of X chromosome activity in two incontinentia pigmenti families with probable linkage to Xq28.
    Curtis AR, Lindsay S, Boye E, Clarke AJ, Landy SJ, Bhattacharya SS.
    Eur J Hum Genet; 1994 Sep; 2(1):51-8. PubMed ID: 7913867
    [Abstract] [Full Text] [Related]

  • 8. X-inactivation and marker studies in three families with incontinentia pigmenti: implications for counselling and gene localisation.
    Woffendin H, Jakins T, Jouet M, Stewart H, Landy S, Haan E, Harris A, Donnai D, Read A, Kenwrick S.
    Clin Genet; 1999 Jan; 55(1):55-60. PubMed ID: 10066033
    [Abstract] [Full Text] [Related]

  • 9. A novel PCR approach for prenatal detection of the common NEMO rearrangement in incontinentia pigmenti.
    Steffann J, Raclin V, Smahi A, Woffendin H, Munnich A, Kenwrick SJ, Grebille AG, Benachi A, Dumez Y, Bonnefont JP, Hadj-Rabia S.
    Prenat Diagn; 2004 May; 24(5):384-8. PubMed ID: 15164415
    [Abstract] [Full Text] [Related]

  • 10. Recent progress in the genetics of incontinentia pigmenti (Bloch-Sulzberger syndrome).
    Shastry BS.
    J Hum Genet; 2000 May; 45(6):323-6. PubMed ID: 11185738
    [Abstract] [Full Text] [Related]

  • 11. Linkage of X-linked myopathy with excessive autophagy (XMEA) to Xq28.
    Villard L, des Portes V, Levy N, Louboutin JP, Recan D, Coquet M, Chabrol B, Figarella-Branger D, Chelly J, Pellissier JF, Fontes M.
    Eur J Hum Genet; 2000 Feb; 8(2):125-9. PubMed ID: 10757644
    [Abstract] [Full Text] [Related]

  • 12. X-linked nonspecific mental retardation (MRX16) mapping to distal Xq28: linkage study and neuropsychological data in a large family.
    Gendrot C, Ronce N, Raynaud M, Ayrault AD, Dourlens J, Castelnau P, Muh JP, Chelly J, Moraine C.
    Am J Med Genet; 1999 Apr 23; 83(5):411-8. PubMed ID: 10232754
    [Abstract] [Full Text] [Related]

  • 13. The genetics of incontinentia pigmenti.
    Curth HO, Warburton D.
    Arch Dermatol; 1965 Sep 23; 92(3):229-35. PubMed ID: 11851242
    [Abstract] [Full Text] [Related]

  • 14. Incontinentia pigmenti: Xp breakpoint is not the same in a case of r(X) and in X/autosome translocations.
    Sefiani A, Heuertz S, Turleau C, Thibaud D, de Grouchy J, Hors-Cayla MC.
    Ann Genet; 1989 Sep 23; 32(3):149-51. PubMed ID: 2817774
    [Abstract] [Full Text] [Related]

  • 15. Cosmids map two incontinentia pigmenti type 1 (IP1) translocation breakpoints to a 180-kb region within a 1.2-Mb YAC contig.
    Gorski JL, Bialecki MD, McDonald MT, Massa HF, Trask BJ, Burright EN.
    Genomics; 1996 Jul 15; 35(2):338-45. PubMed ID: 8661147
    [Abstract] [Full Text] [Related]

  • 16. Gonadal mosaicism for incontinentia pigmenti in a healthy male.
    Kirchman TT, Levy ML, Lewis RA, Kanzler MH, Nelson DL, Scheuerle AE.
    J Med Genet; 1995 Nov 15; 32(11):887-90. PubMed ID: 8592334
    [Abstract] [Full Text] [Related]

  • 17. Linkage studies do not confirm the cytogenetic location of incontinentia pigmenti on Xp11.
    Sefiani A, Sinnett D, Abel L, Szpiro-Tapia S, Heuertz S, Craig I, Fraser N, Kruse TA, Frydman M, Peter MO.
    Hum Genet; 1988 Nov 15; 80(3):282-6. PubMed ID: 3192215
    [Abstract] [Full Text] [Related]

  • 18. Linkage analysis of bipolar illness with X-chromosome DNA markers: a susceptibility gene in Xq27-q28 cannot be excluded.
    De bruyn A, Raeymaekers P, Mendelbaum K, Sandkuijl LA, Raes G, Delvenne V, Hirsch D, Staner L, Mendlewicz J, Van Broeckhoven C.
    Am J Med Genet; 1994 Dec 15; 54(4):411-9. PubMed ID: 7726217
    [Abstract] [Full Text] [Related]

  • 19. Regional localization of two MRX genes to Xq28 (MRX28) and to Xp11.4-Xp22.12 (MRX33).
    Holinski-Feder E, Golla A, Rost I, Seidel H, Rittinger O, Meindl A.
    Am J Med Genet; 1996 Jul 12; 64(1):125-30. PubMed ID: 8826462
    [Abstract] [Full Text] [Related]

  • 20. Genetic screening for hemophilia A (classic hemophilia) with a polymorphic DNA probe.
    Oberle I, Camerino G, Heilig R, Grunebaum L, Cazenave JP, Crapanzano C, Mannucci PM, Mandel JL.
    N Engl J Med; 1985 Mar 14; 312(11):682-6. PubMed ID: 2983207
    [Abstract] [Full Text] [Related]

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