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

237 related items for PubMed ID: 4141590

  • 21. The chromosomal constitution of 165 human translocations involving D group chromosomes identified by autoradiography.
    Cohen MM.
    Ann Genet; 1971 Jun; 14(2):87-96. PubMed ID: 4254302
    [No Abstract] [Full Text] [Related]

  • 22. Down's syndrome at young maternal age; cytogenetical and genealogical study of eighty-two families.
    Mikkelson M.
    Ann Hum Genet; 1967 Aug; 31(1):51-69. PubMed ID: 4228454
    [No Abstract] [Full Text] [Related]

  • 23. Human cytogenetics: trends and techniques.
    Porter IH.
    Prog Clin Pathol; 1973 Aug; 5():19-48. PubMed ID: 4131375
    [No Abstract] [Full Text] [Related]

  • 24. Down syndrome associated with a familial 14/21 translocation.
    Hanna EJ, Johnston WP, Nevin NC.
    Ulster Med J; 1981 Aug; 50(2):95-8. PubMed ID: 6460372
    [No Abstract] [Full Text] [Related]

  • 25. Down's syndrome associated with a familial (21q-; 22q+) translocation.
    Cohen MM, Davidson RG.
    Cytogenetics; 1967 Aug; 6(5):321-30. PubMed ID: 4231490
    [No Abstract] [Full Text] [Related]

  • 26. [Incidence of association of acrocentric chromosomes].
    Krajewska-Walasek M.
    Pediatr Pol; 1980 Jan; 55(1):9-14. PubMed ID: 6445056
    [No Abstract] [Full Text] [Related]

  • 27. [Cytogenetic studies in children with Down's syndrome and in their relatives].
    Ostojska J.
    Pediatr Pol; 1972 Oct; 47(10):1231-8. PubMed ID: 4263834
    [No Abstract] [Full Text] [Related]

  • 28. Inherited pericentric inversion of Y-chromosome with trisomy 21. A case report.
    Krishna Murthy DS, Murthy SK, Patel JK, Banker GN, Shah VC.
    Ann Genet; 1989 Oct; 32(1):47-51. PubMed ID: 2526612
    [Abstract] [Full Text] [Related]

  • 29. Unusual chromosome aberrations in 3 children with Down syndrome.
    Osztovics M, Tóth S, Wilhelm O.
    Acta Paediatr Acad Sci Hung; 1982 Oct; 23(3):283-9. PubMed ID: 6217717
    [Abstract] [Full Text] [Related]

  • 30. A de novo translocation, 14q21q, with a microchromosome-14p21p.
    Abeliovich D, Katz M, Karplus M, Carmi R.
    Am J Med Genet; 1985 Sep; 22(1):29-33. PubMed ID: 2931981
    [Abstract] [Full Text] [Related]

  • 31. [2 children of the same mother with Down's syndrome. Cytogenetic and genealogic analysis of the family].
    Kalicanin P, Marković V, Morić-Petrović S, Despotović M.
    Srp Arh Celok Lek; 1970 May; 98(5):737-48. PubMed ID: 4253281
    [No Abstract] [Full Text] [Related]

  • 32. [Translocation t(2q-; 21q+) in three generations].
    Laurent C, Robert JM.
    Ann Genet; 1968 Mar; 11(1):28-32. PubMed ID: 4233292
    [No Abstract] [Full Text] [Related]

  • 33. [The intelligence level in the chromosome aberrations affecting autosomes].
    Moor L.
    Rev Neuropsychiatr Infant; 1970 Dec; 18(12):943-66. PubMed ID: 4251821
    [No Abstract] [Full Text] [Related]

  • 34. Probable reciprocal translocation in somatic cells from patients with Down's syndrome.
    Sonta S, Oishi H.
    Jinrui Idengaku Zasshi; 1974 Sep; 19(2):169-73. PubMed ID: 4280457
    [No Abstract] [Full Text] [Related]

  • 35. Induction of distinctive chromosomal bands in selected human subjects with D, G, and Y chromosome anomalies.
    Kakati S, Sinha AK.
    Hum Hered; 1973 Apr; 23(4):313-30. PubMed ID: 4130026
    [No Abstract] [Full Text] [Related]

  • 36. [Ovarian stimulation, amniocentesis and prenatal chromosome analysis in a l4-21 translocation carrier with secondary amenorrhea].
    Philip J, Lebech P, Niebuhr E, Mikkelsen M.
    Ugeskr Laeger; 1972 Aug 28; 134(35):1850-2. PubMed ID: 4262957
    [No Abstract] [Full Text] [Related]

  • 37. Diverse chromosomal anomalies in a family.
    Atkins L, Bartsocas CS, Porter PJ.
    J Med Genet; 1968 Dec 28; 5(4):314-8. PubMed ID: 4238963
    [No Abstract] [Full Text] [Related]

  • 38. Simultaneous occurrence of ring "G" chromosome and group "B" pericentric inversion in the same individual: case report and review of the literature.
    Singer H, Scaife NS.
    Pediatrics; 1970 Jul 28; 46(1):74-83. PubMed ID: 5423459
    [No Abstract] [Full Text] [Related]

  • 39. Cytogenetic studies on mongols in Singapore.
    Boon WH, Seng CT.
    J Singapore Paediatr Soc; 1969 Apr 28; 11(1):8-24. PubMed ID: 4243834
    [No Abstract] [Full Text] [Related]

  • 40. The Philadelphia chromosome.
    Baserga A, Castoldi GL.
    Biomedicine; 1973 Mar 28; 18(2):89-94. PubMed ID: 4125985
    [No Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 12.