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

Journal Abstract Search


174 related items for PubMed ID: 6218140

  • 21. [Relationship between dermatoglyphic variability and finger length in genetic disorders: Down's syndrome].
    Mglinets VA.
    Genetika; 1991 Mar; 27(3):541-7. PubMed ID: 1830282
    [Abstract] [Full Text] [Related]

  • 22.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 23.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 24. Parental dermatoglyphics in Down's syndrome. A ten-year study.
    Priest JH, Verhulst C, Sirkin S.
    J Med Genet; 1973 Dec; 10(4):328-32. PubMed ID: 4272738
    [Abstract] [Full Text] [Related]

  • 25.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 26.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 27. Evaluation of dermal patterns in Down's syndrome by predictive discrimination. I. Preliminary analysis based on frequencies of patterns.
    Borgaonkar DS, Davis M, Bolling DR, Herr HM.
    Johns Hopkins Med J; 1971 Mar; 128(3):141-52. PubMed ID: 4251839
    [No Abstract] [Full Text] [Related]

  • 28. Karyotypic analysis of 150 cases of Down's Syndrome in Iraq.
    Ferman A, Shakir A.
    J Ment Defic Res; 1976 Jun; 20(2):83-7. PubMed ID: 133247
    [Abstract] [Full Text] [Related]

  • 29. Incidence of Down's syndrome in Sweden during the years 1968-1977.
    Lindsten J, Marsk L, Berglund K, Iselius L, Ryman N, Annerén G, Kjessler B, Mitelman F, Nordenson I, Wahlström J, Vejlens L.
    Hum Genet Suppl; 1981 Jun; 2():195-210. PubMed ID: 6218136
    [Abstract] [Full Text] [Related]

  • 30.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 31. Double aneuploidy: partial trisomy 21 and XO/XXX in a family with 12/21 translocation.
    Chen H, Tyrkus M, Woolley PV.
    Ann Genet; 1978 Sep; 21(3):177-80. PubMed ID: 315194
    [Abstract] [Full Text] [Related]

  • 32.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 33.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 34. Cytogenetic studies of a family with trisomy 21 mosaicism in two successive generations as the cause of Down's syndrome.
    Werner W, Herrmann FH, John B.
    Hum Genet; 1982 Sep; 60(2):202-4. PubMed ID: 6210621
    [No Abstract] [Full Text] [Related]

  • 35.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 36.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 37.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 38. Comparison of mental development in individuals with mosaic and trisomy 21 Down's syndrome.
    Fishler K, Koch R, Donnell GN.
    Pediatrics; 1976 Nov; 58(5):744-8. PubMed ID: 135957
    [Abstract] [Full Text] [Related]

  • 39. Decreasing mosaicism in Down's syndrome.
    Wilson MG, Towner JW, Forsman I.
    Clin Genet; 1980 May; 17(5):335-40. PubMed ID: 6449318
    [Abstract] [Full Text] [Related]

  • 40. [Bilateral symmetry of the dermatoglyphic characteristics in Down's syndrome].
    Mglinets VA, Ivanov VI.
    Ontogenez; 1993 May; 24(3):98-102. PubMed ID: 8355961
    [Abstract] [Full Text] [Related]


    Page: [Previous] [Next] [New Search]
    of 9.