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Journal Abstract Search

226 related items for PubMed ID: 4340312

  • 1. [Hereditary skin diseases related to sex].
    Desmons F, Walbaum R.
    Lille Med; 1972 Mar; 17(3):447-70. PubMed ID: 4340312
    [No Abstract] [Full Text] [Related]

  • 2. [Genetic counseling in dermatology].
    Stoll C, Grosshans EM.
    Minerva Med; 1972 Dec 15; 63(90):4961-8. PubMed ID: 4345325
    [No Abstract] [Full Text] [Related]

  • 3. Hereditary syndromes with auditory and dermatological manifestations.
    Reed WB, Stone VM, Boder E, Ziprkowski L.
    Arch Dermatol; 1967 May 15; 95(5):456-61. PubMed ID: 4164668
    [No Abstract] [Full Text] [Related]

  • 4. Ichthyosis linearis circumflexa comèl. A clinico-statistical approach to its relationship with Netherton's syndrome.
    Mevorah B, Frenk E, Brooke EM.
    Dermatologica; 1974 May 15; 149(4):201-9. PubMed ID: 4480416
    [No Abstract] [Full Text] [Related]

  • 5. [X-chromosome-linked hereditary dermatoses].
    Happle R.
    Hautarzt; 1982 Feb 15; 33(2):73-81. PubMed ID: 6804414
    [Abstract] [Full Text] [Related]

  • 6. Ichthyosis linearis circumflexa comèl with trichorrhexis invaginata (Netherton's syndrome). A light microscopical study of the skin changes.
    Mevorah B, Frenk E.
    Dermatologica; 1974 Feb 15; 149(4):193-200. PubMed ID: 4480415
    [No Abstract] [Full Text] [Related]

  • 7. [Netherton's syndrome. Ichthyosis-like changes in the skin and trichorrhexis invaginata. Demonstration of pathologically changed cortex keratin in the hair].
    Orfanos CE, Mahrle G, Salamon T.
    Hautarzt; 1971 Sep 15; 22(9):397-409. PubMed ID: 5172063
    [No Abstract] [Full Text] [Related]

  • 8. [Genetic counseling in dermatology].
    Blanchet-Bardon C.
    Rev Prat; 1985 Nov 21; 35(53):3225-30. PubMed ID: 3936159
    [No Abstract] [Full Text] [Related]

  • 9. [Cytogenetic studies on some rarer dermatoses].
    Back F, Maestri D.
    Hautarzt; 1966 Jan 21; 17(1):35-6. PubMed ID: 4963733
    [No Abstract] [Full Text] [Related]

  • 10. Sparse hair, short stature, hypoplastic thumbs, single upper central incisor and abnormal skin pigmentation: a possible "new" form of ectodermal dysplasia.
    Winter RM, MacDermot KD, Hill FJ.
    Am J Med Genet; 1988 Jan 21; 29(1):209-16. PubMed ID: 3344769
    [Abstract] [Full Text] [Related]

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  • 12. Basal cell carcinomas, coarse sparse hair, and milia.
    Oley CA, Sharpe H, Chenevix-Trench G.
    Am J Med Genet; 1992 Jul 15; 43(5):799-804. PubMed ID: 1642265
    [No Abstract] [Full Text] [Related]

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  • 14. Familial epidermodysplasia verruciformis of Lewandowsky and Lutz.
    Rajagopalan K, Bahru J, Loo DS, Tay CH, Chin KN, Tan KK.
    Arch Dermatol; 1972 Jan 15; 105(1):73-8. PubMed ID: 5009624
    [No Abstract] [Full Text] [Related]

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  • 17. Hereditary acrokeratotic poikiloderma.
    Weary PE, Manley WF, Graham GF.
    Arch Dermatol; 1971 Apr 15; 103(4):409-22. PubMed ID: 4253719
    [No Abstract] [Full Text] [Related]

  • 18. VI. Birth defects and genetic disorders.
    J Invest Dermatol; 1979 Nov 15; 73(5 Pt 2):460-72. PubMed ID: 115930
    [No Abstract] [Full Text] [Related]

  • 19. Nertherton's syndrome.
    Brodin MB, Porter PS.
    Cutis; 1980 Aug 15; 26(2):185-8, 191. PubMed ID: 6893301
    [Abstract] [Full Text] [Related]

  • 20. Skin manifestations in visceral cancer.
    Andreev VC.
    Curr Probl Dermatol; 1978 Aug 15; 8():1-168. PubMed ID: 359256
    [No Abstract] [Full Text] [Related]

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