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488 related items for PubMed ID: 20045761

  • 1. Unbalanced and balanced acrocentric rearrangements involving chromosomes other than chromosome 21 at amniocentesis.
    Chen CP, Chern SR, Wu PC, Tsai FJ, Lee CC, Town DD, Chen WL, Chen LF, Lee MS, Pan CW, Wang W.
    Taiwan J Obstet Gynecol; 2009 Dec; 48(4):389-99. PubMed ID: 20045761
    [Abstract] [Full Text] [Related]

  • 2. Unbalanced and balanced heterologous acrocentric rearrangements involving chromosome 21 at amniocentesis.
    Chen CP, Chern SR, Wu PC, Tsai FJ, Lee CC, Town DD, Chen WL, Chen LF, Lee MS, Pan CW, Wang W.
    Taiwan J Obstet Gynecol; 2010 Mar; 49(1):62-8. PubMed ID: 20466295
    [Abstract] [Full Text] [Related]

  • 3. Molecular studies of translocations and trisomy involving chromosome 13.
    Robinson WP, Bernasconi F, Dutly F, Lefort G, Romain DR, Binkert F, Schinzel AA.
    Am J Med Genet; 1996 Jan 11; 61(2):158-63. PubMed ID: 8669444
    [Abstract] [Full Text] [Related]

  • 4. Uniparental disomy in fetuses diagnosed with balanced Robertsonian translocations: risk estimate.
    Silverstein S, Lerer I, Sagi M, Frumkin A, Ben-Neriah Z, Abeliovich D.
    Prenat Diagn; 2002 Aug 11; 22(8):649-51. PubMed ID: 12210570
    [Abstract] [Full Text] [Related]

  • 5. Risks of unbalanced progeny at amniocentesis to carriers of chromosome rearrangements: data from United States and Canadian laboratories.
    Daniel A, Hook EB, Wulf G.
    Am J Med Genet; 1989 May 11; 33(1):14-53. PubMed ID: 2750783
    [Abstract] [Full Text] [Related]

  • 6. The importance of investigating for uniparental disomy in prenatally identified balanced acrocentric rearrangements.
    McGowan KD, Weiser JJ, Horwitz J, Berend SA, McCaskill C, Sutton VR, Shaffer LG.
    Prenat Diagn; 2002 Feb 11; 22(2):141-3. PubMed ID: 11857621
    [Abstract] [Full Text] [Related]

  • 7. Parental origin determination in thirty de novo Robertsonian translocations.
    Shaffer LG, Jackson-Cook CK, Stasiowski BA, Spence JE, Brown JA.
    Am J Med Genet; 1992 Aug 01; 43(6):957-63. PubMed ID: 1357969
    [Abstract] [Full Text] [Related]

  • 8. Prenatal search for UPD 14 and UPD 15 in 83 cases of familial and de novo heterologous Robertsonian translocations.
    Ruggeri A, Dulcetti F, Miozzo M, Grati FR, Grimi B, Bellato S, Natacci F, Maggi F, Simoni G.
    Prenat Diagn; 2004 Dec 15; 24(12):997-1000. PubMed ID: 15614836
    [Abstract] [Full Text] [Related]

  • 9. Prenatally diagnosed balanced chromosome rearrangements: eight years' experience.
    Peng HH, Chao AS, Wang TH, Chang YL, Chang SD.
    J Reprod Med; 2006 Sep 15; 51(9):699-703. PubMed ID: 17039698
    [Abstract] [Full Text] [Related]

  • 10. 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 15; 16(4):323-32. PubMed ID: 8734806
    [Abstract] [Full Text] [Related]

  • 11. Incidence and significance of chromosome mosaicism involving an autosomal structural abnormality diagnosed prenatally through amniocentesis: a collaborative study.
    Hsu LY, Yu MT, Richkind KE, Van Dyke DL, Crandall BF, Saxe DF, Khodr GS, Mennuti M, Stetten G, Miller WA, Priest JH.
    Prenat Diagn; 1996 Jan 15; 16(1):1-28. PubMed ID: 8821848
    [Abstract] [Full Text] [Related]

  • 12. Unbalanced reciprocal translocations at amniocentesis.
    Chen CP, Wu PC, Lin CJ, Chern SR, Tsai FJ, Lee CC, Town DD, Chen WL, Chen LF, Lee MS, Pan CW, Wang W.
    Taiwan J Obstet Gynecol; 2011 Mar 15; 50(1):48-57. PubMed ID: 21482375
    [Abstract] [Full Text] [Related]

  • 13. 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]

  • 14. Combined use of cytogenetic analysis and FISH for the identification of two antenatal de novo markers as Robertsonian translocations involving the p arms.
    Pierluigi M, Battaglia P, Perfumo C, Baroncini A, Bricarelli FD.
    Ann Genet; 1997 Feb 15; 40(2):99-103. PubMed ID: 9259956
    [Abstract] [Full Text] [Related]

  • 15. Dual-color fish analysis of breakpoints on Robertsonian translocations.
    Takahashi Y, Fujita H, Nakamura Y, Kurahashi H.
    Jpn J Hum Genet; 1997 Dec 15; 42(4):517-23. PubMed ID: 9560951
    [Abstract] [Full Text] [Related]

  • 16. Recombinant balanced and unbalanced translocations as a consequence of a balanced complex chromosomal rearrangement involving eight breakpoints in four chromosomes.
    Röthlisberger B, Kotzot D, Brecevic L, Koehler M, Balmer D, Binkert F, Schinzel A.
    Eur J Hum Genet; 1999 Dec 15; 7(8):873-83. PubMed ID: 10602362
    [Abstract] [Full Text] [Related]

  • 17. Prenatally diagnosed de novo apparently balanced complex chromosome rearrangements: two new cases and review of the literature.
    Ruiz C, Grubs RE, Jewett T, Cox-Jones K, Abruzzese E, Pettenati MJ, Rao PN.
    Am J Med Genet; 1996 Aug 23; 64(3):478-84. PubMed ID: 8862625
    [Abstract] [Full Text] [Related]

  • 18. Identification of uniparental disomy in phenotypically abnormal carriers of isochromosomes or Robertsonian translocations.
    Berend SA, Bejjani BA, McCaskill C, Shaffer LG.
    Am J Med Genet; 2002 Sep 01; 111(4):362-5. PubMed ID: 12210293
    [Abstract] [Full Text] [Related]

  • 19. Molecular cytogenetic characterization of 17 rob(13q14q) Robertsonian translocations by FISH, narrowing the region containing the breakpoints.
    Han JY, Choo KH, Shaffer LG.
    Am J Hum Genet; 1994 Nov 01; 55(5):960-7. PubMed ID: 7977359
    [Abstract] [Full Text] [Related]

  • 20. Biparental inheritance of chromosome 21 polymorphic markers indicates that some Robertsonian translocations t(21;21) occur postzygotically.
    Blouin JL, Binkert F, Antonarakis SE.
    Am J Med Genet; 1994 Feb 01; 49(3):363-8. PubMed ID: 8209906
    [Abstract] [Full Text] [Related]

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