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

157 related items for PubMed ID: 5492689

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

  • 2. [Autosomal chromosome aberrations].
    Serville F, Battin J.
    Bord Med; 1971 May; 4(5):1373-416. PubMed ID: 5105683
    [No Abstract] [Full Text] [Related]

  • 3. Mosaic supernumerary small ring chromosome.
    Fryns JP, van Herck G, van den Berghe H.
    J Genet Hum; 1981 Jun; 29(2):151-4. PubMed ID: 7328409
    [No Abstract] [Full Text] [Related]

  • 4. Structural abnormalities of chromosome 18. 3. Two G-18 translocations, one identified AS 22-18.
    Fraccaro M, Herin P, Hultén M, Ivemark BI, Jonasson J, Lindsten J, Tiepolo L, Zetterqvist P.
    Ann Genet; 1972 Jun; 15(2):93-8. PubMed ID: 4537728
    [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. Familial structural chromosome abnormality with maternal mosaicism.
    Insley J, McDermott A, Parrington J.
    Ann Genet; 1968 Sep; 11(3):138-44. PubMed ID: 5304613
    [No Abstract] [Full Text] [Related]

  • 10. [A chemical and karyological study in a case of dyscraniotic oligophrenia].
    Caldarini G, Paracchi G.
    Folia Hered Pathol (Milano); 1968 Jul; 17(3):103-12. PubMed ID: 5732581
    [No Abstract] [Full Text] [Related]

  • 11. Monosomy G mosaicism in twonrelated children.
    Schulz J, Krmpotic E.
    J Ment Defic Res; 1968 Dec; 12(4):255-67. PubMed ID: 5729526
    [No Abstract] [Full Text] [Related]

  • 12. Mosaic normal/15q11-q13 duplication associated with developmental delay but normal phenotype.
    Goossens E, Decock P, Potgieter S, Fryns JP.
    Genet Couns; 1999 Dec; 10(2):133-6. PubMed ID: 10422005
    [Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14. Phenotype/karyotype correlations of Y chromosome aneuploidy with emphasis on structural aberrations in postnatally diagnosed cases.
    Hsu LY.
    Am J Med Genet; 1994 Nov 01; 53(2):108-40. PubMed ID: 7856637
    [Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No 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. 18q- and 18q+ mosaicism in a mentally retarded boy.
    Ausems MG, Bhola SL, Post-Blok CA, Hennekam RC, de France HF.
    Am J Med Genet; 1994 Nov 15; 53(3):296-9. PubMed ID: 7856666
    [Abstract] [Full Text] [Related]

  • 20. Clinical, cytogeneti and autoradiographic studies in 0 cases with rare chromosome disorders. IV. Cases 9 and 10.
    Moore MK, Engel E.
    Ann Genet; 1970 Dec 15; 13(4):269-74. PubMed ID: 5313392
    [No Abstract] [Full Text] [Related]

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