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Journal Abstract Search

64 related items for PubMed ID: 1733165

  • 1. Tentative assignment of gene for oto-palato-digital syndrome to distal Xq (Xq26-q28).
    Hoar DI, Field LL, Beards F, Hoganson G, Rollnick B, Hoo JJ.
    Am J Med Genet; 1992 Jan 15; 42(2):170-2. PubMed ID: 1733165
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  • 5. Oto-palato-digital syndrome type I: further evidence for assignment of the locus to Xq28.
    Biancalana V, Le Marec B, Odent S, van den Hurk JA, Hanauer A.
    Hum Genet; 1991 Dec 15; 88(2):228-30. PubMed ID: 1757098
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  • 6. Linkage localization of Börjeson-Forssman-Lehmann syndrome.
    Mathews KD, Ardinger HH, Nishimura DY, Buetow KH, Murray JC, Bartley JA.
    Am J Med Genet; 1989 Dec 15; 34(4):470-4. PubMed ID: 2624254
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  • 7. Further linkage data on Norrie disease.
    Kivlin JD, Sanborn GE, Wright E, Cannon L, Carey J.
    Am J Med Genet; 1987 Mar 15; 26(3):733-6. PubMed ID: 3565487
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  • 8. Mapping a gene for familial situs abnormalities to human chromosome Xq24-q27.1.
    Casey B, Devoto M, Jones KL, Ballabio A.
    Nat Genet; 1993 Dec 15; 5(4):403-7. PubMed ID: 8298651
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  • 13. Multiple congenital anomalies associated with an oto-palato-digital syndrome type II.
    Blanchet P, Lefort G, Eglin MC, Rieu D, Sarda P.
    Genet Couns; 1993 Dec 15; 4(4):289-94. PubMed ID: 8110417
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  • 14. Mapping the gene for X-linked cataracts and microcornea with facial, dental, and skeletal features to Xp22: an appraisal of the Nance-Horan syndrome.
    Lewis RA.
    Trans Am Ophthalmol Soc; 1989 Dec 15; 87():658-728. PubMed ID: 2576480
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  • 18. Refinement of the background genetic map of Xq26-q27 and gene localisation for Börjeson-Forssman-Lehmann Syndrome.
    Gedeon AK, Kozman HM, Robinson H, Pilia G, Schlessinger D, Turner G, Mulley JC.
    Am J Med Genet; 1996 Jul 12; 64(1):63-8. PubMed ID: 8826450
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  • 19. 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
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