These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

150 related items for PubMed ID: 9664211

  • 1. Trisomy 8 mosaicism: a further five cases illustrating marked clinical and cytogenetic variability.
    Jordan MA, Marques I, Rosendorff J, de Ravel TJ.
    Genet Couns; 1998; 9(2):139-46. PubMed ID: 9664211
    [Abstract] [Full Text] [Related]

  • 2. Supernumerary marker chromosomes 5: confirmation of a critical region and resultant phenotype.
    D'Amato Sizonenko L, Ng D, Oei P, Winship I.
    Am J Med Genet; 2002 Jul 22; 111(1):19-26. PubMed ID: 12124728
    [Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5. Molecular and cytogenetic characterisation of an unusual case of partial trisomy/partial monosomy 13 mosaicism: 46,XX,r(13)(p11q14)/46,XX,der(13)t(13;13)(q10;q14).
    Gentile M, Buonadonna AL, Cariola F, Fiorente P, Valenzano MC, Guanti G.
    J Med Genet; 1999 Jan 22; 36(1):77-82. PubMed ID: 9950374
    [Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8. Mosaicism for a chromosome 8-derived minute marker chromosome in a patient with manifestations of trisomy 8 mosaicism.
    Spinner NB, Grace KR, Owens NL, Sovinsky L, Pellegrino JE, McDonald-McGinn D, Zackai E.
    Am J Med Genet; 1995 Mar 13; 56(1):22-4. PubMed ID: 7747780
    [Abstract] [Full Text] [Related]

  • 9. Duplication 12q mosaicism in two unrelated patients with a similar syndrome.
    Harrod MJ, Byrne JB, Dev VG, Francke U.
    Am J Med Genet; 1980 Mar 13; 7(2):123-9. PubMed ID: 7468644
    [Abstract] [Full Text] [Related]

  • 10. Asymmetric clinical and cytogenetic findings in a 4-year-old girl with trisomy 18 mosaicism.
    Rao KW, Buchanan PD, Aylsworth AS.
    Birth Defects Orig Artic Ser; 1978 Mar 13; 14(6C):349-54. PubMed ID: 728589
    [No Abstract] [Full Text] [Related]

  • 11. [Phenotype positioning on chromosomes in a patient with the syndrome of partial trisomy 7p21.2-->pter].
    Liang DS, Wu LQ, Cai F, Xia K, Long ZG, Pan Q, Dai HP, Xia JH.
    Yi Chuan Xue Bao; 2005 Feb 13; 32(2):124-9. PubMed ID: 15759858
    [Abstract] [Full Text] [Related]

  • 12. Prenatally detected trisomy 4 and 6 mosaicism--cytogenetic results and clinical phenotype.
    Wieczorek D, Prott EC, Robinson WP, Passarge E, Gillessen-Kaesbach G.
    Prenat Diagn; 2003 Feb 13; 23(2):128-33. PubMed ID: 12575019
    [Abstract] [Full Text] [Related]

  • 13. Unique mosaicism of tetraploidy and trisomy 8: clinical, cytogenetic, and molecular findings in a live-born infant.
    Roberts HE, Saxe DF, Muralidharan K, Coleman KB, Zacharias JF, Fernhoff PM.
    Am J Med Genet; 1996 Mar 29; 62(3):243-6. PubMed ID: 8882781
    [Abstract] [Full Text] [Related]

  • 14. Cryptic mosaicism for monosomy 20 identified in renal tract cells.
    Stefanou EG, Crocker M, Boon A, Stewart H.
    Clin Genet; 2006 Sep 29; 70(3):228-32. PubMed ID: 16922725
    [Abstract] [Full Text] [Related]

  • 15. Unilateral microtia in an infant with trisomy 18 mosaicism.
    Giannatou E, Leze H, Katana A, Kolialexi A, Mavrou A, Kanavakis E, Kitsiou-Tzeli S.
    Genet Couns; 2009 Sep 29; 20(2):181-7. PubMed ID: 19650416
    [Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19. Common trisomy mosaicism diagnosed in amniocytes involving chromosomes 13, 18, 20 and 21: karyotype-phenotype correlations.
    Wallerstein R, Yu MT, Neu RL, Benn P, Lee Bowen C, Crandall B, Disteche C, Donahue R, Harrison B, Hershey D, Higgins RR, Jenkins LS, Jackson-Cook C, Keitges E, Khodr G, Lin CC, Luthardt FW, Meisner L, Mengden G, Patil SR, Rodriguez M, Sciorra LJ, Shaffer LG, Stetten G, Van Dyke DL, Wang H.
    Prenat Diagn; 2000 Feb 29; 20(2):103-22. PubMed ID: 10694683
    [Abstract] [Full Text] [Related]

  • 20. Constitutional partial 1q trisomy mosaicism and Wilms tumor.
    Mark HF, Wyandt H, Pan A, Milunsky JM.
    Cancer Genet Cytogenet; 2005 Oct 15; 162(2):166-71. PubMed ID: 16213366
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 8.