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Journal Abstract Search

121 related items for PubMed ID: 17726694

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  • 3. A novel phenotype characterized by digital abnormalities, intellectual disability, and short stature in a Mexican family maps to Xp11.4-p11.21.
    Barboza-Cerda MC, Campos-Acevedo LD, Rangel R, Martínez-de-Villarreal LE, Déctor MA.
    Am J Med Genet A; 2013 Feb; 161A(2):237-43. PubMed ID: 23307567
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  • 6. Alport syndrome. Molecular genetic aspects.
    Hertz JM.
    Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
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  • 9. Genetic heterogeneity of FG syndrome: a fourth locus (FGS4) maps to Xp11.4-p11.3 in an Italian family.
    Piluso G, Carella M, D'Avanzo M, Santinelli R, Carrano EM, D'Avanzo A, D'Adamo AP, Gasparini P, Nigro V.
    Hum Genet; 2003 Feb; 112(2):124-30. PubMed ID: 12522552
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  • 12. Additional case of Keipert syndrome and review of the literature.
    Cappon SM, Khalifa MM.
    Med Sci Monit; 2000 Feb; 6(4):776-8. PubMed ID: 11208408
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  • 15. A family with X-linked deafness showing linkage to the proximal Xq region of the X chromosome.
    Robinson D, Lamont M, Curtis G, Shields DC, Phelps P.
    Hum Genet; 1992 Nov; 90(3):316-8. PubMed ID: 1362559
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  • 18. 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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