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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

129 related items for PubMed ID: 1611908

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  • 27. DXS26 (HU16) is located in Xq21.1.
    Sankila EM, Bruns GA, Schwartz M, Nikoskelainen E, Niebuhr E, Hodgson SV, Wright AF, de la Chapelle A.
    Hum Genet; 1990 Jun; 85(1):117-20. PubMed ID: 2162804
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  • 28. Fine mapping of X-linked clasped thumb and mental retardation (MASA syndrome) in Xq28.
    Legius E, Kaepernick L, Higgins JV, Glover TW.
    Clin Genet; 1994 Apr; 45(4):165-8. PubMed ID: 8062432
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  • 30. Linkage relationships of human arginine vasopressin-neurophysin-II and oxytocin-neurophysin-I to prodynorphin and other loci on chromosome 20.
    Summar ML, Phillips JA, Battey J, Castiglione CM, Kidd KK, Maness KJ, Weiffenbach B, Gravius TC.
    Mol Endocrinol; 1990 Jun; 4(6):947-50. PubMed ID: 1978246
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  • 31. 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; 88(2):228-30. PubMed ID: 1757098
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  • 37. Localization of the gene for Wieacker-Wolff syndrome in the pericentromeric region of the X chromosome.
    Kloos DU, Jakubiczka S, Wienker T, Wolff G, Wieacker P.
    Hum Genet; 1997 Sep; 100(3-4):426-30. PubMed ID: 9272167
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  • 39. X-linked mental retardation.
    Turner G.
    Psychol Med; 1982 Aug; 12(3):471-3. PubMed ID: 6957904
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  • 40. Centre d'etude du polymorphisme humain (CEPH): collaborative genetic mapping of the human genome.
    Dausset J, Cann H, Cohen D, Lathrop M, Lalouel JM, White R.
    Genomics; 1990 Mar; 6(3):575-7. PubMed ID: 2184120
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