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350 related items for PubMed ID: 12224075

  • 1. Prenatal and postnatal characterization of Y chromosome structural anomalies by molecular cytogenetic analysis.
    Hernando C, Carrera M, Ribas I, Parear N, Baraibar R, Egocue J, Fuster C.
    Prenat Diagn; 2002 Sep; 22(9):802-5. PubMed ID: 12224075
    [Abstract] [Full Text] [Related]

  • 2. Prenatal diagnosis of mos46,X,del(Y)(q11.2)/45,X by cytogenetic and molecular studies with multiplex STR analysis.
    Hwa HL, Ko TM, Chang YY, Huang CH, Su YN, Tseng LH, Hsieh FJ.
    Prenat Diagn; 2004 Feb; 24(2):121-4. PubMed ID: 14974120
    [Abstract] [Full Text] [Related]

  • 3. Isodicentric Y (p11.32) chromosome in an infant with mixed gonadal dysgenesis.
    Aktas D, Alikasifoglu M, Gonc N, Senocak ME, Tuncbilek E.
    Eur J Med Genet; 2006 Feb; 49(2):141-9. PubMed ID: 16530711
    [Abstract] [Full Text] [Related]

  • 4. [Delineation of three structural Y chromosome aberrations combined molecular techniques].
    Tu XD, Zeng J, Cong XW, Yan AZ, Huang WJ, Lin YH, Zheng DZ, Zhang M, Wang ZH.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2013 Aug; 30(4):420-4. PubMed ID: 23926008
    [Abstract] [Full Text] [Related]

  • 5. Clinical and molecular cytogenetic studies in three infertile patients with mosaic rearranged Y chromosomes.
    Bettio D, Venci A, Rizzi N, Negri L, Setti PL.
    Hum Reprod; 2006 Apr; 21(4):972-5. PubMed ID: 16484313
    [Abstract] [Full Text] [Related]

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  • 7. Prenatal detection and characterization of a small supernumerary marker chromosome (sSMC) derived from chromosome 22 with apparently normal phenotype.
    Lin CC, Hsieh YY, Wang CH, Li YC, Hsieh LJ, Lee CC, Tsai CH, Tsai FJ.
    Prenat Diagn; 2006 Oct; 26(10):898-902. PubMed ID: 16915592
    [Abstract] [Full Text] [Related]

  • 8. A dysmorphic newborn with 45,X,der(1)inv(1)(p13;qter)t(Y;1)(pter-->q11;p13),-Y de novo karyotype.
    Tatar A, Oztas S, Yakut T, Ors R.
    Genet Couns; 2005 Oct; 16(2):173-7. PubMed ID: 16080298
    [Abstract] [Full Text] [Related]

  • 9. Prenatal diagnosis and molecular cytogenetic analysis of partial monosomy 10q (10q25.3-->qter) and partial trisomy 18q (18q23-->qter) in a fetus associated with cystic hygroma and ambiguous genitalia.
    Chen CP, Chern SR, Wang TH, Hsueh DW, Lee CC, Town DD, Wang W, Ko TM.
    Prenat Diagn; 2005 Jun; 25(6):492-6. PubMed ID: 15966044
    [Abstract] [Full Text] [Related]

  • 10. [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; 26(4):461-4. PubMed ID: 20017317
    [Abstract] [Full Text] [Related]

  • 11. [Cytogenetic and molecular genetic analysis of a case with mosaic marker chromosomes].
    Tu X, Zeng J, Cong X, Zhang X, Yan A.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Feb; 33(1):76-80. PubMed ID: 26829740
    [Abstract] [Full Text] [Related]

  • 12. Dynamic mosaicism manifesting as loss, gain and rearrangement of an isodicentric Y chromosome in a male child with growth retardation and abnormal external genitalia.
    Iourov IY, Vorsanova SG, Liehr T, Monakhov VV, Soloviev IV, Yurov YB.
    Cytogenet Genome Res; 2008 Feb; 121(3-4):302-6. PubMed ID: 18758177
    [Abstract] [Full Text] [Related]

  • 13. Prenatal diagnosis of mos45,X/46,X,+mar in a fetus with normal male external genitalia and a literature review.
    Chien SC, Chen CP, Lin CC, Huang LC, Hsieh CT, Tsai FJ.
    Taiwan J Obstet Gynecol; 2009 Sep; 48(3):292-5. PubMed ID: 19797023
    [Abstract] [Full Text] [Related]

  • 14. Molecular and cytogenetic characterization of a structural rearrangement of the Y chromosome in an azoospermic man.
    Valetto A, Bertini V, Rapalini E, Baldinotti F, Di Martino D, Simi P.
    Fertil Steril; 2004 May; 81(5):1388-90. PubMed ID: 15136108
    [Abstract] [Full Text] [Related]

  • 15. Array-CGH characterization of a prenatally detected de novo 46,X,der(Y)t(X;Y)(p22.3;q11.2) in a male fetus.
    Palka C, Alfonsi M, Morizio E, Soranno A, La Rovere D, Matarrelli B, Rullo AL, Zori R, Chiarelli F, Calabrese G.
    Eur J Med Genet; 2011 May; 54(3):333-6. PubMed ID: 21354345
    [Abstract] [Full Text] [Related]

  • 16. Crypt Y chromosome fragment resulting from an X;Y translocation in a patient with premature ovarian failure.
    Cheng DH, Tan YQ, Di YF, Li LY, Lu GX.
    Fertil Steril; 2009 Aug; 92(2):828.e3-6. PubMed ID: 19524892
    [Abstract] [Full Text] [Related]

  • 17. Phenotype/karyotype correlations of Y chromosome aneuploidy with emphasis on structural aberrations in postnatally diagnosed cases.
    Hsu LY.
    Am J Med Genet; 1994 Nov 01; 53(2):108-40. PubMed ID: 7856637
    [Abstract] [Full Text] [Related]

  • 18. [Screening for Y chromosome sequences in patients with Turner syndrome].
    Ferrão L, Lopes ML, Limbert C, Marques B, Boieiro F, Silva M, Marques R, Lavinha J, Mota A, Gonçalves J.
    Acta Med Port; 2002 Nov 01; 15(2):89-100. PubMed ID: 15524154
    [Abstract] [Full Text] [Related]

  • 19. Characterization of a de novo unbalanced Y;autosome translocation in a 45,X mentally retarded male and literature review.
    Chen CP, Lin SP, Tsai FJ, Wang TH, Chern SR, Wang W.
    Fertil Steril; 2008 Oct 01; 90(4):1198.e11-8. PubMed ID: 18304539
    [Abstract] [Full Text] [Related]

  • 20. Evidence of a mechanism for isodicentric chromosome Y formation in a 45,X/46,X,idic(Y)(p11.31)/46,X,del(Y)(p11.31) mosaic karyotype.
    Reshmi SC, Miller JL, Deplewski D, Close C, Henderson LJ, Littlejohn E, Schwartz S, Waggoner DJ.
    Eur J Med Genet; 2011 Oct 01; 54(2):161-4. PubMed ID: 21078420
    [Abstract] [Full Text] [Related]

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