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Journal Abstract Search

331 related items for PubMed ID: 2370045

  • 21.
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  • 22. Primary amenorrhea with Xq duplication.
    Rajangam S, Lincoln S, Tilak P, Thomas IM.
    Indian J Med Sci; 1999 Feb; 53(2):49-52. PubMed ID: 10798023
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  • 23. Large inverted repeats within Xp11.2 are present at the breakpoints of isodicentric X chromosomes in Turner syndrome.
    Scott SA, Cohen N, Brandt T, Warburton PE, Edelmann L.
    Hum Mol Genet; 2010 Sep 01; 19(17):3383-93. PubMed ID: 20570968
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  • 25. Short stature homeobox-containing gene duplication on the der(X) chromosome in a female with 45,X/46,X, der(X), gonadal dysgenesis, and tall stature.
    Ogata T, Kosho T, Wakui K, Fukushima Y, Yoshimoto M, Miharu N.
    J Clin Endocrinol Metab; 2000 Aug 01; 85(8):2927-30. PubMed ID: 10946905
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  • 29. Short stature in a mother and daughter caused by familial der(X)t(X;X)(p22.1-3;q26).
    Reinehr T, Jauch A, Zoll B, Engel U, Bartels I, Andler W.
    Am J Med Genet; 2001 Jul 22; 102(1):81-5. PubMed ID: 11471178
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  • 30. Partial short arm deletion of the X chromosome 46,X,del(X)(qter = to p21:).
    Käosaar M, Mikelsaar AV.
    Hum Genet; 1980 Feb 22; 53(2):275-7. PubMed ID: 7358395
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  • 31.
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  • 32. Cognition and the sex chromosomes: studies in Turner syndrome.
    Ross J, Roeltgen D, Zinn A.
    Horm Res; 2006 Feb 22; 65(1):47-56. PubMed ID: 16397401
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  • 33.
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  • 35. Molecular cytogenetic characterization of two Turner syndrome patients with mosaic ring X chromosome.
    Chauhan P, Jaiswal SK, Lakhotia AR, Rai AK.
    J Assist Reprod Genet; 2016 Sep 22; 33(9):1161-8. PubMed ID: 27387888
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  • 38. Familial Turner syndrome.
    Verschraegen-Spae MR, Depypere H, Speleman F, Dhondt M, De Paepe A.
    Clin Genet; 1992 Apr 22; 41(4):218-20. PubMed ID: 1576760
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  • 40. X chromosome constitution and the human female phenotype.
    Therman E, Denniston C, Sarto GE, Ulber M.
    Hum Genet; 1980 Apr 22; 54(2):133-43. PubMed ID: 7390488
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