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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

112 related items for PubMed ID: 3621639

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  • 3. Autosomal recessive onychotrichodysplasia, chronic neutropenia and mild mental retardation. Delineation of the syndrome.
    Hernández A, Olivares F, Cantú JM.
    Clin Genet; 1979 Feb; 15(2):147-52. PubMed ID: 761414
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  • 4. A case of onycotricodysplasia with intellectual disability, without neutropenia.
    Ikbal M, Eker HK, Tos T, Alp MY, Cebi AH.
    Genet Couns; 2012 Feb; 23(3):389-92. PubMed ID: 23072187
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  • 8. Alopecia totalis, nail dysplasia and amelogenesis imperfecta.
    Gorlin RJ, Cervenka J.
    Birth Defects Orig Artic Ser; 1975 Feb; 11(5):23-4. PubMed ID: 1218220
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  • 14. Lazy leukocyte syndrome in a black infant.
    Aggarwal J, Khan AJ, Diamond S, Schaeffer HA, Evans HE.
    J Natl Med Assoc; 1985 Nov; 77(11):928-9. PubMed ID: 4078918
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  • 15. T cell lymphocytosis with neutropenia.
    Murray JA, Lilleyman JS.
    Arch Dis Child; 1983 Aug; 58(8):635-6. PubMed ID: 6604500
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  • 16. [Congenital dystrophy of the pigment layer of the posterior pole with congenital total hypotrichosis (author's transl)].
    Kroll P.
    Klin Monbl Augenheilkd; 1981 Feb; 178(2):118-20. PubMed ID: 7230692
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  • 17. Cronkhite-Canada syndrome: report of a case with bacteriologic, immunologic, and electron microscopic studies.
    Ali M, Weinstein J, Biempica L, Halpern A, Das KM.
    Gastroenterology; 1980 Oct; 79(4):731-6. PubMed ID: 7409392
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  • 19. Esophageal ulcers in immunodeficiency with elevated levels of IgM and neutropenia.
    Vanderhoof JA, Rich KC, Stiehm ER, Ament ME.
    Am J Dis Child; 1977 May; 131(5):551-2. PubMed ID: 855839
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  • 20. [Hypotrichosis congenita hereditaria Maria Unna].
    Wirth G, Bindewald I, Küster W, Goerz G.
    Hautarzt; 1985 Oct; 36(10):577-80. PubMed ID: 4066319
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