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Journal Abstract Search

63 related items for PubMed ID: 11594343

  • 21. 46,XX gonadal dysgenesis with epibulbar dermoid.
    Quayle SA, Copeland KC.
    Am J Med Genet; 1991 Jul 01; 40(1):75-6. PubMed ID: 1909490
    [Abstract] [Full Text] [Related]

  • 22. Narrowing the map of a gene (MRXS9) for X-linked mental retardation, microcephaly, and variably short stature at Xq12-q21.31.
    Shrimpton AE, Braddock BR, Hoo JJ.
    Am J Med Genet; 2000 May 15; 92(2):155-6. PubMed ID: 10797443
    [No Abstract] [Full Text] [Related]

  • 23. Gene localization for oral-facial-digital syndrome type 1 (OFD1:MIM 311200) proximal to DXS85.
    Gedeon AK, Oley C, Nelson J, Turner G, Mulley JC.
    Am J Med Genet; 1999 Feb 12; 82(4):352-4. PubMed ID: 10051172
    [No Abstract] [Full Text] [Related]

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  • 25. [A case of corneal limbal dermoid].
    Tanaka K.
    Nihon Ganka Kiyo; 1972 Jan 12; 23(1):90-1. PubMed ID: 5062609
    [No Abstract] [Full Text] [Related]

  • 26. 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 12; 8(2):125-9. PubMed ID: 10757644
    [Abstract] [Full Text] [Related]

  • 27. Ultrastructural study of Norrie's disease.
    Van Nouhuys CE.
    Am J Ophthalmol; 1991 Oct 15; 112(4):475-7. PubMed ID: 1928264
    [No Abstract] [Full Text] [Related]

  • 28. Localization of CSNBX (CSNB4) between the retinitis pigmentosa loci RP2 and RP3 on proximal Xp.
    Hardcastle AJ, David-Gray ZK, Jay M, Bird AC, Bhattacharya SS.
    Invest Ophthalmol Vis Sci; 1997 Dec 15; 38(13):2750-5. PubMed ID: 9418727
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  • 30. 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 Dec 15; 5(3):168-70. PubMed ID: 9272741
    [Abstract] [Full Text] [Related]

  • 31. A new X linked recessive deafness syndrome with blindness, dystonia, fractures, and mental deficiency is linked to Xq22.
    Tranebjaerg L, Schwartz C, Eriksen H, Andreasson S, Ponjavic V, Dahl A, Stevenson RE, May M, Arena F, Barker D.
    J Med Genet; 1995 Apr 15; 32(4):257-63. PubMed ID: 7643352
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  • 33. 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
    [Abstract] [Full Text] [Related]

  • 34. [Contribution to the study of the heredity of epibulbar dermoids].
    Proto F, Scullica L.
    Acta Genet Med Gemellol (Roma); 1966 Oct 15; 15(4):351-63. PubMed ID: 5971712
    [No Abstract] [Full Text] [Related]

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  • 38. X-linked mental retardation associated with cleft lip/palate maps to Xp11.3-q21.3.
    Siderius LE, Hamel BC, van Bokhoven H, de Jager F, van den Helm B, Kremer H, Heineman-de Boer JA, Ropers HH, Mariman EC.
    Am J Med Genet; 1999 Jul 30; 85(3):216-20. PubMed ID: 10398231
    [Abstract] [Full Text] [Related]

  • 39. Linkage analysis in three families with nonspecific X-linked mental retardation.
    Claes S, Gu XX, Legius E, Lorenzetti E, Marynen P, Fryns JP, Cassiman JJ, Raeymaekers P.
    Am J Med Genet; 1996 Jul 12; 64(1):137-46. PubMed ID: 8826464
    [Abstract] [Full Text] [Related]

  • 40. Optic nerve teratoma and odontogenic dermoid cyst in a neonate with persistent fetal vasculature.
    Guirgis MF, White FV, Dunbar JA, Smith ME, Lueder GT.
    Arch Ophthalmol; 2002 Nov 12; 120(11):1582-5. PubMed ID: 12427078
    [No Abstract] [Full Text] [Related]

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