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Journal Abstract Search

484 related items for PubMed ID: 14974122

  • 1. Prenatal diagnosis of the distal 11q deletion and review of the literature.
    Chen CP, Chern SR, Chang TY, Tzen CY, Lee CC, Chen WL, Chen LF, Wang W.
    Prenat Diagn; 2004 Feb; 24(2):130-6. PubMed ID: 14974122
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  • 2. 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; 26(2):138-46. PubMed ID: 16470734
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  • 5. Prenatal diagnosis of mosaicism for 11q terminal deletion.
    Valduga M, Cannard VL, Philippe C, Romana S, Miton A, Droulle P, Foliguet B, Lecompte T, Jonveaux P.
    Eur J Med Genet; 2007 Feb; 50(6):475-81. PubMed ID: 17761465
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  • 6. Prenatal diagnosis of a deletion of 18q in a fetus associated with multiple-marker screen positive results.
    Chen CP, Chern SR, Liu FF, Jan SW, Lee CC, Chang YC, Yue CT.
    Prenat Diagn; 1997 Jun; 17(6):571-6. PubMed ID: 9203216
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  • 8. Clinical, cytogenetic, and molecular findings of prenatally diagnosed mosaic trisomy 4.
    Chen CP, Chern SR, Lee CC, Chang TY, Wang W, Tzen CY.
    Prenat Diagn; 2004 Jan; 24(1):38-44. PubMed ID: 14755408
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  • 10. 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; 50(1):67-73. PubMed ID: 21482378
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  • 11. Prenatal diagnosis and molecular cytogenetic characterization of a de novo interstitial duplication of 11q (11q22.3→q23.3) associated with abnormal maternal serum biochemistry.
    Chen CP, Su YN, Lin SP, Chern SR, Su JW, Chen YT, Lee MS, Wang W.
    Taiwan J Obstet Gynecol; 2013 Mar; 52(1):120-4. PubMed ID: 23548232
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  • 12. 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
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  • 13. 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; 25(6):451-5. PubMed ID: 15966060
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  • 14. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from ring chromosome 4.
    Chen CP, Chen M, Su YN, Tsai FJ, Chern SR, Wu PC, Chen WL, Chen LF, Pan CW, Wang W.
    Taiwan J Obstet Gynecol; 2011 Jun; 50(2):188-95. PubMed ID: 21791306
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  • 16. De novo 7q deletion with a positive maternal serum triple test screening.
    Park IY, Jo YS, Shin JC, Sung IK, Kim M.
    J Obstet Gynaecol Res; 2008 Feb; 34(1):85-7. PubMed ID: 18226135
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  • 18. Prenatal findings and molecular cytogenetic analyses of partial trisomy 12q (12q24.32-->qter) and partial monosomy 21q (21q22.2-->qter).
    Chen CP, Chern SR, Lin CC, Wang TH, Li YC, Hsieh LJ, Lee CC, Hua HM, Wang W.
    Prenat Diagn; 2006 Apr; 26(4):313-20. PubMed ID: 16506269
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  • 19. Prenatal diagnosis of trisomy 18p and distal 21q22.3 deletion.
    Chen CP, Chern SR, Lee CC, Chen LF, Chin DT, Tzen CY, Wang W.
    Prenat Diagn; 2003 Sep; 23(9):758-61. PubMed ID: 12975789
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