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

148 related items for PubMed ID: 3874593

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

  • 4. Prenatal diagnosis and characterization of an analphoid marker chromosome 16.
    Tabet AC, Gosset P, Elghezal H, Fontaine S, Martinovic J, Encha Razavi F, Romana S, Vekemans M, Morichon-Delvallez N.
    Prenat Diagn; 2004 Sep; 24(9):733-6. PubMed ID: 15386469
    [Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6. Complete trisomy 17p a relatively new syndrome.
    Martsolf JT, Larson L, Jalal SM, Wasdahl WA, Miller R, Kukolich M.
    Ann Genet; 1988 Sep; 31(3):172-4. PubMed ID: 3066280
    [Abstract] [Full Text] [Related]

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

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9. The phenotypic and cytogenetic spectrum of partial trisomy 9.
    Wilson GN, Raj A, Baker D.
    Am J Med Genet; 1985 Feb; 20(2):277-82. PubMed ID: 3976721
    [Abstract] [Full Text] [Related]

  • 10. [Partial trisomy of the long arm of chromosome 2 by malsegregation of a maternal translocation t(2;7)(q321;p22)].
    Siffroi JP, Romani F, Viguié F, Lejeune C.
    Ann Genet; 1984 Feb; 27(4):241-4. PubMed ID: 6335372
    [Abstract] [Full Text] [Related]

  • 11. Trisomy 8 syndrome. A report of 2 cases.
    Ioan D, Dumitriu L, Muşeţeanu P, Belengeanu V, Pop T, Maximilian C.
    Endocrinologie; 1986 Feb; 24(1):45-8. PubMed ID: 3961414
    [Abstract] [Full Text] [Related]

  • 12. [Clinical spectrum and congenital anomalies in trisomy 18].
    Arizawa M, Nakayama M, Suehara N.
    Nihon Sanka Fujinka Gakkai Zasshi; 1989 Oct; 41(10):1545-50. PubMed ID: 2584807
    [Abstract] [Full Text] [Related]

  • 13. Limb reduction defects and renal dysplasia: confirmation of a new, apparently lethal, autosomal recessive MCA syndrome.
    Schrander-Stumpel C, de Die-Smulders C, Fryns JP, da Costa J, Bouckaert P.
    Am J Med Genet; 1990 Sep; 37(1):133-5. PubMed ID: 2240030
    [Abstract] [Full Text] [Related]

  • 14. Clinical delineation of trisomy 9 syndrome.
    Katayama KP, Wilkinson EJ, Herrmann J, Glaspey JC, Agarwal AB, Roesler MR, Mattingly RF.
    Obstet Gynecol; 1980 Nov; 56(5):665-8. PubMed ID: 7432742
    [Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16. Trisomy for the short arm of chromosome 10. Report of a new case resulting from segregation of a maternal balanced translocation t(10qter----q11::14p11----qter).
    Delaroche I, Bruni L, Giannotti A, Giampaolo R, Aebischer ML.
    Helv Paediatr Acta; 1984 May; 39(2):161-6. PubMed ID: 6543839
    [Abstract] [Full Text] [Related]

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

  • 18. [Mosaic trisomy 14 due to an iso dicentric chromosome (author's transl)].
    Turleau C, de Grouchy J, Cornu A, Turquet M, Millet G.
    Ann Genet; 1980 May; 23(4):238-40. PubMed ID: 6971604
    [Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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