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207 related items for PubMed ID: 21914491

  • 1. Clinical and molecular description of a fetus in prenatal diagnosis with a rare de novo ring 10 and deletions of 12.59 Mb in 10p15.3-p14 and 4.22 Mb in 10q26.3.
    Christopoulou G, Tzetis M, Konstantinidou AE, Tsezou A, Kanavakis E, Kitsiou-Tzeli S, Velissariou V.
    Eur J Med Genet; 2012 Jan; 55(1):75-9. PubMed ID: 21914491
    [Abstract] [Full Text] [Related]

  • 2. Wolf-Hirschhorn (4p-) syndrome: prenatal diagnosis, molecular cytogenetic characterization and association with a 1.2-Mb microduplication at 8p22-p21.3 and a 1.1-Mb microduplication at 10p15.3 in a fetus with an apparently pure 4p deletion.
    Chen CP, Su YN, Chen YY, Su JW, Chern SR, Chen YT, Chen WL, Chen LF, Wang W.
    Taiwan J Obstet Gynecol; 2011 Dec; 50(4):506-11. PubMed ID: 22212326
    [Abstract] [Full Text] [Related]

  • 3. A prenatally ascertained, maternally inherited 14.8 Mb duplication of chromosomal bands Xq13.2-q21.31 associated with multiple congenital abnormalities in a male fetus.
    Sismani C, Donoghue J, Alexandrou A, Karkaletsi M, Christopoulou S, Konstantinidou AE, Livanos P, Patsalis PC, Velissariou V.
    Gene; 2013 Nov 01; 530(1):138-42. PubMed ID: 23973723
    [Abstract] [Full Text] [Related]

  • 4. Prenatal detection of a de novo terminal inverted duplication 4p in a fetus with the Wolf-Hirschhorn syndrome phenotype.
    Beaujard MP, Jouannic JM, Bessières B, Borie C, Martin-Luis I, Fallet-Bianco C, Portnoï MF.
    Prenat Diagn; 2005 Jun 01; 25(6):451-5. PubMed ID: 15966060
    [Abstract] [Full Text] [Related]

  • 5. Prenatal diagnosis and molecular cytogenetic characterization of rec(10)dup(10p)inv(10)(p11.2q26.3) in a fetus associated with paternal pericentric inversion.
    Chen CP, Ko TM, Su YN, Wang LK, Chern SR, Wu PS, Chen YN, Chen SW, Ko K, Lee CC, Chen LF, Yang CW, Wang W.
    Taiwan J Obstet Gynecol; 2016 Oct 01; 55(5):733-737. PubMed ID: 27751426
    [Abstract] [Full Text] [Related]

  • 6. Prenatal diagnosis and molecular cytogenetic characterization of mosaic ring chromosome 13.
    Chen CP, Tsai CH, Chern SR, Wu PS, Su JW, Lee CC, Chen YT, Chen WL, Chen LF, Wang W.
    Gene; 2013 Oct 15; 529(1):163-8. PubMed ID: 23933417
    [Abstract] [Full Text] [Related]

  • 7. Pure partial monosomy 3p (3p25.3 → pter): prenatal diagnosis and array comparative genomic hybridization characterization.
    Chen CP, Su YN, Chen CY, Su JW, Chern SR, Town DD, Wang W.
    Taiwan J Obstet Gynecol; 2012 Sep 15; 51(3):435-9. PubMed ID: 23040932
    [Abstract] [Full Text] [Related]

  • 8. Inv dup del(9p): prenatal diagnosis and molecular cytogenetic characterization by fluorescence in situ hybridization and array comparative genomic hybridization.
    Chen CP, Su YN, Chern SR, Hsu CY, Tsai FJ, Wu PC, Lee CC, Chen YT, Lee MS, Wang W.
    Taiwan J Obstet Gynecol; 2011 Mar 15; 50(1):67-73. PubMed ID: 21482378
    [Abstract] [Full Text] [Related]

  • 9. Chromosome 1p32-p31 deletion syndrome: prenatal diagnosis by array comparative genomic hybridization using uncultured amniocytes and association with NFIA haploinsufficiency, ventriculomegaly, corpus callosum hypogenesis, abnormal external genitalia, and intrauterine growth restriction.
    Chen CP, Su YN, Chen YY, Chern SR, Liu YP, Wu PC, Lee CC, Chen YT, Wang W.
    Taiwan J Obstet Gynecol; 2011 Sep 15; 50(3):345-52. PubMed ID: 22030051
    [Abstract] [Full Text] [Related]

  • 10. Prenatal diagnosis of a 9q34.3 microdeletion by array-CGH in a fetus with an apparently balanced translocation.
    Simovich MJ, Yatsenko SA, Kang SH, Cheung SW, Dudek ME, Pursley A, Ward PA, Patel A, Lupski JR.
    Prenat Diagn; 2007 Dec 15; 27(12):1112-7. PubMed ID: 17849500
    [Abstract] [Full Text] [Related]

  • 11. Prenatal diagnosis of de novo t(2;18;14)(q33.1;q12.2;q31.2), dup(5)(q34q34), del(7)(p21.1p21.1), and del(10)(q25.3q25.3) and a review of the prenatally ascertained de novo apparently balanced complex and multiple chromosomal rearrangements.
    Chen CP, Chern SR, Lee CC, Lin CC, Li YC, Hsieh LJ, Chen WL, Wang W.
    Prenat Diagn; 2006 Feb 15; 26(2):138-46. PubMed ID: 16470734
    [Abstract] [Full Text] [Related]

  • 12. Clinical and molecular description of the prenatal diagnosis of a fetus with a maternally inherited microduplication 22q11.2 of 2.5 Mb.
    Christopoulou G, Sismani C, Sakellariou M, Saklamaki M, Athanassiou V, Velissariou V.
    Gene; 2013 Sep 25; 527(2):694-7. PubMed ID: 23506827
    [Abstract] [Full Text] [Related]

  • 13. [Prenatal diagnosis of two fetuses with de novo small supernumerary markers by single nucleotide polymorphism array based comparative genomic hybridization].
    Ji XQ, Li L, Lin Y, Ma DY, Liu A, Zhang JJ, Cheng J, Zhou J, Hu P, Xu ZF.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2012 Oct 25; 29(5):510-4. PubMed ID: 23042383
    [Abstract] [Full Text] [Related]

  • 14. Detection of recurrent 4p16.3 microdeletion with 2p25.3 microduplication by multiplex ligation-dependent probe amplification and array comparative genomic hybridization in a fetus from a family with Wolf-Hirschhorn syndrome.
    Yang WX, Pan H, Wang ST, Li L, Wu HR, Qi Y.
    Taiwan J Obstet Gynecol; 2016 Feb 25; 55(1):104-8. PubMed ID: 26927259
    [Abstract] [Full Text] [Related]

  • 15. Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 8.
    Chen CP, Chen M, Ko TM, Ma GC, Tsai FJ, Tsai MS, Wu PC, Lee CC, Chen LF, Wang W.
    Taiwan J Obstet Gynecol; 2010 Dec 25; 49(4):500-5. PubMed ID: 21199754
    [Abstract] [Full Text] [Related]

  • 16. Genotype-phenotype correlation in 13q13.3-q21.3 deletion.
    Tosca L, Brisset S, Petit FM, Metay C, Latour S, Lautier B, Lebas A, Druart L, Picone O, Mas AE, Prévot S, Tardieu M, Goossens M, Tachdjian G.
    Eur J Med Genet; 2011 Dec 25; 54(5):e489-94. PubMed ID: 21741501
    [Abstract] [Full Text] [Related]

  • 17. Rapid aneuploidy diagnosis of partial trisomy 7q (7q34→qter) and partial monosomy 10q (10q26.12→qter) by array comparative genomic hybridization using uncultured amniocytes.
    Chen CP, Lin SP, Su YN, Tsai FJ, Wu PC, Town DD, Chen LF, Lee MS, Wang W.
    Taiwan J Obstet Gynecol; 2012 Mar 25; 51(1):93-9. PubMed ID: 22482977
    [Abstract] [Full Text] [Related]

  • 18. Prenatal diagnosis of a female fetus with ring chromosome 9, 46,XX,r(9)(p24q34), and a de novo interstitial 9p deletion.
    Penacho V, Galán F, Martín-Bayón TA, Mayo S, Manchón I, Carrasco A, Martínez-Castellano F, Alcaraz LA.
    Cytogenet Genome Res; 2014 Mar 25; 144(4):275-9. PubMed ID: 25722017
    [Abstract] [Full Text] [Related]

  • 19. Prenatal diagnosis and molecular characterization of an interstitial 1q24.3-31.3 deletion: case report and review.
    Prontera P, Clerici G, Bernardini L, Schippa M, Capalbo A, Manes I, Giuffrida MG, Barbieri MG, Ardisia C, Donti E.
    Genet Couns; 2011 Mar 25; 22(1):41-8. PubMed ID: 21614987
    [Abstract] [Full Text] [Related]

  • 20. Inv dup del(10p): Prenatal diagnosis and molecular cytogenetic characterization.
    Chen CP, Ko TM, Wang LK, Chern SR, Wu PS, Chen SW, Wu FT, Chen LF, Wang W.
    Taiwan J Obstet Gynecol; 2019 Sep 25; 58(5):698-703. PubMed ID: 31542096
    [Abstract] [Full Text] [Related]

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