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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

132 related items for PubMed ID: 3570776

  • 21. Congenital localized absence of skin, blistering and nail abnormalities, a new syndrome.
    Bart BJ.
    Birth Defects Orig Artic Ser; 1971 Jun; 7(8):118-20. PubMed ID: 5173254
    [Abstract] [Full Text] [Related]

  • 22. Short stature, brachydactyly, nail dysplasia, and mental retardation: further observation of the Tonoki syndrome.
    Sorge G, Baieli S, Mauceri L, Greco F, Fiumara A.
    Am J Med Genet; 1998 Dec 04; 80(4):403-5. PubMed ID: 9856572
    [Abstract] [Full Text] [Related]

  • 23. Hereditary distal onycholysis--a case report.
    Bazex J, Baran R, Monbrun F, Grigorieff-Larrue N, Marguery MC.
    Clin Exp Dermatol; 1990 Mar 04; 15(2):146-8. PubMed ID: 2347107
    [Abstract] [Full Text] [Related]

  • 24. [Familial clustering of cerebrovascular anomalies].
    Galambos S, Erós E.
    Orv Hetil; 1998 Jan 18; 139(3):131-5. PubMed ID: 9467296
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  • 26. Corneal changes, hyperkeratosis, short stature, brachydactyly, and premature birth: a new autosomal dominant syndrome.
    Stern JK, Lubinsky MS, Durrie DS, Luckasen JR.
    Am J Med Genet; 1984 May 18; 18(1):67-77. PubMed ID: 6234802
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  • 29. Autosomal dominant onychodystrophy and anonychia with type B brachydactyly and ectrodactyly.
    Kumar D, Levick RK.
    Clin Genet; 1986 Sep 18; 30(3):219-25. PubMed ID: 3780038
    [Abstract] [Full Text] [Related]

  • 30. Symmetric acroleukopathy in mother and daughter.
    Sugai T, Saito T, Hamada T.
    Arch Dermatol; 1965 Aug 18; 92(2):172-3. PubMed ID: 11850922
    [Abstract] [Full Text] [Related]

  • 31. Hereditary twenty-nail dystrophy in a Sicilian family.
    Pavone L, Li Volti S, Guarneri B, La Rosa M, Sorge G, Incorpora G, Mollica F.
    J Med Genet; 1982 Oct 18; 19(5):337-40. PubMed ID: 7143386
    [Abstract] [Full Text] [Related]

  • 32. A novel locus for ectodermal dysplasia of hairs, nails and teeth type maps to chromosome 18q22.1-22.3.
    Tariq M, Chishti MS, Ali G, Ahmad W.
    Ann Hum Genet; 2008 Jan 18; 72(Pt 1):19-25. PubMed ID: 18184143
    [Abstract] [Full Text] [Related]

  • 33. Familial Hirschsprung's disease and type D brachydactyly: a report of four affected males in two generations.
    Reynolds JF, Barber JC, Alford BA, Chandler JG, Kelly TE.
    Pediatrics; 1983 Feb 18; 71(2):246-9. PubMed ID: 6823428
    [Abstract] [Full Text] [Related]

  • 34. Congenital anomalies of the nail unit.
    McCarthy DJ.
    Clin Podiatr Med Surg; 1995 Apr 18; 12(2):319-25. PubMed ID: 7600506
    [Abstract] [Full Text] [Related]

  • 35. Hereditary glaucoma: a report of two pedigrees.
    Lee DA, Brubaker RF, Hruska L.
    Ann Ophthalmol; 1985 Dec 18; 17(12):739-41. PubMed ID: 4091373
    [Abstract] [Full Text] [Related]

  • 36. [Deletion of the short arm of chromosome 7].
    Oster J, Lyngbye T, Friedrich U.
    Ugeskr Laeger; 1974 Dec 30; 137(1):37. PubMed ID: 4454099
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  • 37. [Successful conservative therapy of pincer nail syndrome].
    el-Gammal S, Altmeyer P.
    Hautarzt; 1993 Aug 30; 44(8):535-7. PubMed ID: 8376109
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  • 39. Syndactyly type V.
    Robinow M, Johnson GF, Broock GJ.
    Am J Med Genet; 1982 Apr 30; 11(4):475-82. PubMed ID: 6283889
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