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Journal Abstract Search

223 related items for PubMed ID: 20148908

  • 1. Influence of parental origin of the X chromosome on physical phenotypes and GH responsiveness of patients with Turner syndrome.
    Ko JM, Kim JM, Kim GH, Lee BH, Yoo HW.
    Clin Endocrinol (Oxf); 2010 Jul; 73(1):66-71. PubMed ID: 20148908
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  • 3. Clinical significance of the parental origin of the X chromosome in turner syndrome.
    Sagi L, Zuckerman-Levin N, Gawlik A, Ghizzoni L, Buyukgebiz A, Rakover Y, Bistritzer T, Admoni O, Vottero A, Baruch O, Fares F, Malecka-Tendera E, Hochberg Z.
    J Clin Endocrinol Metab; 2007 Mar; 92(3):846-52. PubMed ID: 17192299
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  • 4. The influence of parental origin of X chromosome genes on the stature of patients with 45 X Turner syndrome.
    Kochi C, Longui CA, Lemos-Marini SH, Guerra-Junior G, Melo MB, Calliari LE, Monte O.
    Genet Mol Res; 2007 Jan 18; 6(1):1-7. PubMed ID: 17278084
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  • 5. Genomic imprinting in Turner syndrome: effects on response to growth hormone and on risk of sensorineural hearing loss.
    Hamelin CE, Anglin G, Quigley CA, Deal CL.
    J Clin Endocrinol Metab; 2006 Aug 18; 91(8):3002-10. PubMed ID: 16757526
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  • 6. Parental origin of normal X chromosomes in Turner syndrome patients with various karyotypes: implications for the mechanism leading to generation of a 45,X karyotype.
    Uematsu A, Yorifuji T, Muroi J, Kawai M, Mamada M, Kaji M, Yamanaka C, Momoi T, Nakahata T.
    Am J Med Genet; 2002 Aug 01; 111(2):134-9. PubMed ID: 12210339
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  • 7. Impact of parental origin of X-chromosome on clinical and biochemical profile in Turner syndrome.
    Malhotra R, Shukla R, Kabra M, Gupta Y, Jyotsna VP, Khadgawat R.
    J Pediatr Endocrinol Metab; 2020 Sep 25; 33(9):1155-1163. PubMed ID: 32813677
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  • 8. Height gains in response to growth hormone treatment to final height are similar in patients with SHOX deficiency and Turner syndrome.
    Blum WF, Cao D, Hesse V, Fricke-Otto S, Ross JL, Jones C, Quigley CA, Binder G.
    Horm Res; 2009 Sep 25; 71(3):167-72. PubMed ID: 19188742
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  • 11. [Identification and characterization of marker chromosome in Turner syndrome].
    Tan YQ, Cheng DH, DI YF, Li LY, Lu GX.
    Zhonghua Fu Chan Ke Za Zhi; 2007 Oct 25; 42(10):679-82. PubMed ID: 18241543
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  • 14. X-chromosome gene dosage as a determinant of impaired pre and postnatal growth and adult height in Turner syndrome.
    Fiot E, Zenaty D, Boizeau P, Haigneré J, Dos Santos S, Léger J, French Turner Syndrome Study Group.
    Eur J Endocrinol; 2016 Mar 25; 174(3):281-8. PubMed ID: 26744895
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  • 15. Paternally derived der(7)t(Y;7)(p11.1 approximately 11.2;p22.3)dn in a mosaic case with Turner syndrome.
    Polityko AD, Khurs OM, Kulpanovich AI, Mosse KA, Solntsava AV, Rumyantseva NV, Naumchik IV, Liehr T, Weise A, Mkrtchyan H.
    Eur J Med Genet; 2009 Mar 25; 52(4):207-10. PubMed ID: 19375526
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  • 16. Gonadoblastoma in Turner syndrome patients with nonmosaic 45,X karyotype and Y chromosome sequences.
    Canto P, Kofman-Alfaro S, Jiménez AL, Söderlund D, Barrón C, Reyes E, Méndez JP, Zenteno JC.
    Cancer Genet Cytogenet; 2004 Apr 01; 150(1):70-2. PubMed ID: 15041227
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  • 17. Parental origin and mechanism of formation of a 46,X,der(X)(pter-->q21.1::p11.4-->pter)/45,X karyotype in a woman with mild Turner syndrome.
    Binkert F, Spreiz A, Höckner M, Miny P, von Dach Leu B, Erdel M, Zschocke J, Utermann G, Kotzot D.
    Fertil Steril; 2010 Jun 01; 94(1):350.e12-5. PubMed ID: 20117774
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  • 18. Ascertainment bias in Turner syndrome: new insights from girls who were diagnosed incidentally in prenatal life.
    Gunther DF, Eugster E, Zagar AJ, Bryant CG, Davenport ML, Quigley CA.
    Pediatrics; 2004 Sep 01; 114(3):640-4. PubMed ID: 15342833
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  • 19. [Analysis of the small supernumerary marker chromosome in Turner syndrome with 45, X/46, X, + mar karyotype].
    Ye ZC, Cai JG, Zhu XY, Zhao R, He XY, Zhong Y, Liu KX, Zhu YM.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Aug 01; 26(4):461-4. PubMed ID: 20017317
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  • 20. Treatment outcome in Turner syndrome.
    Parvin M, Roche E, Costigan C, Hoey HM.
    Ir Med J; 2004 Jan 01; 97(1):12, 14-5. PubMed ID: 15055914
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