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133 related items for PubMed ID: 8183834

  • 1. Prenatal identification of an isochromosome for the short arm of the Y i(Yp), by cytogenetic and molecular analyses.
    Slim R, Soulié J, Hotmar J, Lecolier B, Bercau G, Bernheim A.
    Prenat Diagn; 1994 Jan; 14(1):23-8. PubMed ID: 8183834
    [Abstract] [Full Text] [Related]

  • 2. Prenatal identification of mos 45,X/46,X,+mar in a normal male baby by cytogenetic and molecular analysis.
    Hoshi N, Tonoki H, Handa Y, Fujino T, Okuyama K, Koga Y, Matsumoto Y, Yamada T, Yamada H, Kishida T, Sagawa T, Fujieda K, Nakahori Y, Kant JA, Fujimoto S.
    Prenat Diagn; 1998 Dec; 18(12):1316-22. PubMed ID: 9885026
    [Abstract] [Full Text] [Related]

  • 3. Prenatal identification of i(Yp) by molecular cytogenetic analysis.
    Wang BB, Yu LC, Peng W, Falk RE, Williams J.
    Prenat Diagn; 1995 Dec; 15(12):1115-9. PubMed ID: 8750290
    [Abstract] [Full Text] [Related]

  • 4. 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]

  • 5. Prenatal diagnosis of two rare de novo structural aberrations of the Y chromosome: cytogenetic and molecular analysis.
    Velissariou V, Antoniadi T, Patsalis P, Christopoulou S, Hatzipouliou A, Donoghue J, Bakou K, Kaminopetros P, Athanassiou V, Petersen MB.
    Prenat Diagn; 2001 Jun; 21(6):484-7. PubMed ID: 11438955
    [Abstract] [Full Text] [Related]

  • 6. Prenatal application of fluorescent in situ hybridization (FISH) for identification of a mosaic Y-chromosome marker, idic(Yp).
    Bernstein R, Steinhaus KA, Cain MJ.
    Prenat Diagn; 1992 Sep; 12(9):709-16. PubMed ID: 1438065
    [Abstract] [Full Text] [Related]

  • 7. Application of molecular cytogenetic techniques to characterize the aberrant Y chromosome arising de novo in a male fetus with mosaic 45,X and solve the discrepancy between karyotyping, chromosome microarray, and multiplex ligation dependent probe amplification.
    Lin SY, Lee CN, Peng AY, Yuan TJ, Lee DJ, Lin WH, Ma GC, Chen M.
    J Formos Med Assoc; 2018 Nov; 117(11):1027-1031. PubMed ID: 29752043
    [Abstract] [Full Text] [Related]

  • 8. Prenatal diagnosis of 45,X and 45,X mosaicism: the need for thorough cytogenetic and clinical evaluations.
    Huang B, Thangavelu M, Bhatt S, J Sandlin C, Wang S.
    Prenat Diagn; 2002 Feb; 22(2):105-10. PubMed ID: 11857613
    [Abstract] [Full Text] [Related]

  • 9. Prenatal diagnosis of sex chromosome mosaicism with two marker chromosomes in three cell lines and a review of the literature.
    Zheng J, Yang X, Lu H, Guan Y, Yang F, Xu M, Li M, Ji X, Wang Y, Hu P, Zhou Y.
    Mol Med Rep; 2019 Mar; 19(3):1791-1796. PubMed ID: 30592288
    [Abstract] [Full Text] [Related]

  • 10. FISH, PCR and cytogenetic characterization in a girl with ambiguous genitalia and karyotype mos46,X,iso(Y)(qter-->p11.3::p11.3-->qter)[80]/45,X[17]/46,X,+mar[3].
    Pereira SR, Pereira AC, Souza MT, Ramos MR.
    Genet Mol Res; 2008 Oct 21; 7(4):1089-96. PubMed ID: 19048487
    [Abstract] [Full Text] [Related]

  • 11. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 16.
    Chen CP, Ko TM, Chern SR, Wu PS, Chen SW, Lai ST, Yang CW, Pan CW, Wang W.
    Taiwan J Obstet Gynecol; 2017 Aug 21; 56(4):545-549. PubMed ID: 28805616
    [Abstract] [Full Text] [Related]

  • 12. 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 21; 22(9):802-5. PubMed ID: 12224075
    [Abstract] [Full Text] [Related]

  • 13. Detection of no isochromosome 20q by interphase fluorescent in situ hybridization on uncultured amniocytes in a pregnancy with mosaic isochromosome 20q in cultured amniocytes at amniocentesis.
    Chen CP, Su JW, Chern SR, Kuo YL, Wu PS, Lee MS, Yang CW, Wang W.
    Taiwan J Obstet Gynecol; 2015 Feb 21; 54(1):58-61. PubMed ID: 25675921
    [Abstract] [Full Text] [Related]

  • 14. [Genetic analysis of a fetus with with 45,X/46,X,idic(Y)(q11.2) mosaicism].
    Pan F, Zhang W, Zhang W.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2024 Aug 10; 41(8):897-902. PubMed ID: 39097269
    [Abstract] [Full Text] [Related]

  • 15. Cytogenetic and molecular characterization of two isodicentric Y chromosomes.
    Stankiewicz P, Hélias-Rodzewicz Z, Jakubów-Durska K, Bocian E, Obersztyn E, Rappold GA, Mazurczak T.
    Am J Med Genet; 2001 Jun 01; 101(1):20-5. PubMed ID: 11343332
    [Abstract] [Full Text] [Related]

  • 16. Cytogenetic and molecular investigations of an abnormal Y chromosome: evidence for a pseudo-dicentric (Yq) isochromosome.
    Savary JB, Vasseur F, Flactif M, Willatt L, Lefebvre J, Ferguson-Smith MA, Deminatti MM.
    Ann Genet; 1992 Jun 01; 35(3):134-9. PubMed ID: 1466561
    [Abstract] [Full Text] [Related]

  • 17. Fluorescent in-situ hybridization (FISH) as an aid to marker chromosome identification in prenatal diagnosis.
    Amiel A, Fejgin M, Appelman Z, Shapiro I, Gaber E, Bachar A, Zamir R, Kedar I, Golbus M.
    Eur J Obstet Gynecol Reprod Biol; 1995 Mar 01; 59(1):103-7. PubMed ID: 7781851
    [Abstract] [Full Text] [Related]

  • 18. [Identification of Y chromosome material in an XX male by means of fluorescent in situ hybridization].
    Brandt CA, Hindkjaer J, Strømkjaer H, Christensen MF, Kølvraa S.
    Ugeskr Laeger; 1992 Nov 16; 154(47):3321-4. PubMed ID: 1462437
    [Abstract] [Full Text] [Related]

  • 19. Rapid positive confirmation of mosaicism for a small supernumerary marker chromosome as r(8) by interphase fluorescence in situ hybridization, quantitative fluorescent polymerase chain reaction, and array comparative genomic hybridization on uncultured amniocytes in a pregnancy with fetal pyelectasis.
    Chen CP, Chang SD, Su YN, Chen M, Chern SR, Su JW, Chen YT, Chen WL, Pan CW, Lee MS, Wang W.
    Taiwan J Obstet Gynecol; 2012 Sep 16; 51(3):405-10. PubMed ID: 23040926
    [Abstract] [Full Text] [Related]

  • 20. Molecular, cytogenetic, and clinical characterisation of six XX males including one prenatal diagnosis.
    Margarit E, Soler A, Carrió A, Oliva R, Costa D, Vendrell T, Rosell J, Ballesta F.
    J Med Genet; 1998 Sep 16; 35(9):727-30. PubMed ID: 9733030
    [Abstract] [Full Text] [Related]

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