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

112 related items for PubMed ID: 5153313

  • 1. A D-group monosomy in a lifeborn infant.
    Pelz L.
    Acta Biol Med Ger; 1971; 26(6):1243-5. PubMed ID: 5153313
    [No Abstract] [Full Text] [Related]

  • 2. [Clinical diagnosis of the phenotype corresponding to a ring-shaped D chromosome].
    Rethoré MO, Praud E, Le Loc'h J, Joly C, Saraux H, Aussannaire M, Lejeune J.
    Presse Med (1893); 1970 Apr 25; 78(21):955-8. PubMed ID: 4986088
    [No Abstract] [Full Text] [Related]

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

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

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

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

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

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

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10. [Monosomy 4 p-- (Wolf-Hirschorn's syndrome)].
    Battin J, Channarond J, Génaudeau J, Ruffié M.
    Arch Fr Pediatr; 1977 Nov 25; 34(9):876-81. PubMed ID: 606188
    [Abstract] [Full Text] [Related]

  • 11. The characteristic phenotype of distal 9q3 trisomy is due to duplication of band 9q32.
    Kleczkowska A, Fryns JP, Lemay P, Van den Berghe H.
    Genet Couns; 1993 Nov 25; 4(3):217-21. PubMed ID: 8267931
    [Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13. Aberrant serum protein inheritance in a patient with a ring D chromosome.
    Daniel WL.
    Pediatrics; 1970 Jul 25; 46(1):120-3. PubMed ID: 5423439
    [No Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

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

  • 17. Partial monosomy for a 21 chromosome. Report of a new case of r(21) and review of the literature.
    Ferrante E, Vignetti P, Antonelli M, Bruni L, Bertasi S, Chessa L.
    Helv Paediatr Acta; 1983 Mar 25; 38(1):73-80. PubMed ID: 6345474
    [Abstract] [Full Text] [Related]

  • 18. A pedigree of 4/18 translocation chromosomes with type and countertype partial trisomy and partal monosomy for chromosome 18.
    Valdmanis A, Pearson G, Siegel AE, Hoeksema RH, Mann JD.
    Ann Genet; 1967 Dec 25; 10(4):159-66. PubMed ID: 5301688
    [No Abstract] [Full Text] [Related]

  • 19. Duplication 11p11.3 leads to 14.1 to meiotic crossing--over.
    Strobel RJ, Riccardi VM, Ledbetter DH, Hittner HM.
    Am J Med Genet; 1980 Dec 25; 7(1):15-20. PubMed ID: 7211949
    [Abstract] [Full Text] [Related]

  • 20. Structural abnormalities of chromosome 18. I. A case of 18q-, with autopsy findings.
    Fraccaro M, Hulten M, Ivemark BI, Lindsten J, Tiepolo L, Zetterqvist P.
    Ann Genet; 1971 Dec 25; 14(4):275-80. PubMed ID: 5316132
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 6.