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747 related items for PubMed ID: 14755408

  • 1. 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
    [Abstract] [Full Text] [Related]

  • 2. Prenatal diagnosis of mosaic trisomy 16 associated with congenital diaphragmatic hernia and elevated maternal serum alpha-fetoprotein and human chorionic gonadotrophin.
    Chen CP, Shih JC, Chern SR, Lee CC, Wang W.
    Prenat Diagn; 2004 Jan; 24(1):63-6. PubMed ID: 14755412
    [Abstract] [Full Text] [Related]

  • 3. Prenatal diagnosis of trisomy 3 mosaicism.
    Zaslav AL, Pierno G, Davis J, Fougner A, Jacob J, Kazi R, Blumenthal D, Sturim S, Shaham M, Fox J.
    Prenat Diagn; 2004 Sep; 24(9):693-6. PubMed ID: 15386452
    [Abstract] [Full Text] [Related]

  • 4. Mosaic trisomy 9 at amniocentesis: prenatal diagnosis and molecular genetic analyses.
    Chen CP, Lin HM, Su YN, Chern SR, Tsai FJ, Wu PC, Lee CC, Chen YT, Lee MS, Pan CW, Wang W.
    Taiwan J Obstet Gynecol; 2010 Sep; 49(3):341-50. PubMed ID: 21056321
    [Abstract] [Full Text] [Related]

  • 5. Trisomy 7 mosaicism at amniocentesis: interphase FISH, QF-PCR, and aCGH analyses on uncultured amniocytes for rapid distinguishing of true mosaicism from pseudomosaicism.
    Chen CP, Huang HK, Su YN, Chern SR, Su JW, Lee CC, Town DD, Chen WL, Chen YT, Wang W.
    Taiwan J Obstet Gynecol; 2012 Mar; 51(1):77-82. PubMed ID: 22482973
    [Abstract] [Full Text] [Related]

  • 6. Prenatal diagnosis of mosaic trisomy 2 associated with abnormal maternal serum screening, oligohydramnios, intrauterine growth restriction, ventricular septal defect, preaxial polydactyly, and facial dysmorphism.
    Chen CP, Chen YY, Chern SR, Wu PS, Su JW, Chen YT, Lee CC, Chen LF, Wang W.
    Taiwan J Obstet Gynecol; 2013 Sep; 52(3):395-400. PubMed ID: 24075380
    [Abstract] [Full Text] [Related]

  • 7. Prenatal diagnosis of an infant with mosaic trisomy 16 of paternal origin.
    Paulyson KJ, Sherer DM, Christian SL, Lewis KM, Ledbetter DH, Salafia CM, Meck JM.
    Prenat Diagn; 1996 Nov; 16(11):1021-6. PubMed ID: 8953635
    [Abstract] [Full Text] [Related]

  • 8. 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
    [Abstract] [Full Text] [Related]

  • 9. Prenatal diagnosis of uniparental disomy 15 following trisomy 15 mosaicism.
    Christian SL, Smith AC, Macha M, Black SH, Elder FF, Johnson JM, Resta RG, Surti U, Suslak L, Verp MS, Ledbetter DH.
    Prenat Diagn; 1996 Apr; 16(4):323-32. PubMed ID: 8734806
    [Abstract] [Full Text] [Related]

  • 10. Cytogenetic and molecular genetic characterization of trisomy 20 mosaicism in fetal blood and tissues.
    Micale MA, Wolff DJ, Dickerman LH, Redline R, Conroy JM, Schwartz S.
    Prenat Diagn; 1996 Oct; 16(10):893-7. PubMed ID: 8938057
    [Abstract] [Full Text] [Related]

  • 11. 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
    [Abstract] [Full Text] [Related]

  • 12.
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  • 13. Mosaic deletion-duplication syndrome of chromosome 3: prenatal molecular cytogenetic diagnosis using cultured and uncultured amniocytes and association with fetoplacental discrepancy.
    Chen CP, Su YN, Hsu CY, Chern SR, Lee CC, Chen YT, Chen WL, Wang W.
    Taiwan J Obstet Gynecol; 2011 Dec; 50(4):485-91. PubMed ID: 22212322
    [Abstract] [Full Text] [Related]

  • 14. Dilemma of trisomy 20 mosaicism detected prenatally: is it an innocent finding?
    Reish O, Wolach B, Amiel A, Kedar I, Dolfin T, Fejgin M.
    Am J Med Genet; 1998 Apr 28; 77(1):72-5. PubMed ID: 9557898
    [Abstract] [Full Text] [Related]

  • 15. Trisomy 13 mosaicism: study of serial cytogenetic changes in a case from early pregnancy to infancy.
    Chen M, Yeh GP, Shih JC, Wang BT.
    Prenat Diagn; 2004 Feb 28; 24(2):137-43. PubMed ID: 14974123
    [Abstract] [Full Text] [Related]

  • 16. Double aneuploidy with Edwards-Klinefelter syndromes (48,XXY,+18) of maternal origin: prenatal diagnosis and molecular cytogenetic characterization in a fetus with arthrogryposis of the left wrist and aplasia of the left thumb.
    Chen CP, Chern SR, Chen CY, Wu PC, Chen LF, Pan CW, Wang W.
    Taiwan J Obstet Gynecol; 2011 Dec 28; 50(4):479-84. PubMed ID: 22212321
    [Abstract] [Full Text] [Related]

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  • 18. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from ring chromosome 2.
    Chen CP, Chen M, Chern SR, Wu PS, Chang SP, Lee DJ, Chen YT, Chen LF, Su JW, Hwa-Ruey Hsieh A, Hwa-Jiun Hsieh A, Wang W.
    Taiwan J Obstet Gynecol; 2012 Sep 28; 51(3):411-7. PubMed ID: 23040927
    [Abstract] [Full Text] [Related]

  • 19. Clinical, cytogenetic, and molecular analyses of prenatally diagnosed mosaic tetrasomy for distal chromosome 15q and review of the literature.
    Chen CP, Lin CC, Li YC, Chern SR, Lee CC, Chen WL, Lee MS, Wang W, Tzen CY.
    Prenat Diagn; 2004 Oct 28; 24(10):767-73. PubMed ID: 15503270
    [Abstract] [Full Text] [Related]

  • 20. Prenatal diagnosis of premature centromere division-related mosaic variegated aneuploidy.
    Chen CP, Lee CC, Chen WL, Wang W, Tzen CY.
    Prenat Diagn; 2004 Jan 28; 24(1):19-25. PubMed ID: 14755404
    [Abstract] [Full Text] [Related]

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