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PUBMED FOR HANDHELDS

Journal Abstract Search


169 related items for PubMed ID: 4255243

  • 21. A double aneuploid mosaic: trisomy 13 and XXY.
    Ebbin AJ, Chu Lim R, Towner JW, Wilson MG.
    J Med Genet; 1972 Sep; 9(3):365-7. PubMed ID: 5079108
    [No Abstract] [Full Text] [Related]

  • 22. [Trisomy 21 and trisomy 18 in siblings].
    Girardet P, Grosset L, Juillard E.
    Helv Paediatr Acta; 1972 Dec; 27(6):583-9. PubMed ID: 4265243
    [No Abstract] [Full Text] [Related]

  • 23. [Case of double aneuploidy: trisomy 18 and XXY].
    Bach C, Toublanc JE, Gautier M.
    Ann Genet; 1973 Mar; 16(1):61-6. PubMed ID: 4541812
    [No Abstract] [Full Text] [Related]

  • 24. Cytogenetic abnormalities in orthopedic patients.
    Cowell HR, Clark CE.
    Clin Orthop Relat Res; 1978 Sep; (135):4-14. PubMed ID: 152176
    [Abstract] [Full Text] [Related]

  • 25. Chromosomal conditions in congenital heart disease.
    Dahl G.
    Acta Paediatr Scand; 1970 Jan; 59(1):65-73. PubMed ID: 4247306
    [No Abstract] [Full Text] [Related]

  • 26. [Ocular manifestations of trisomy 18].
    Ardouin M, Urvoy M, Lautridou A, Le Marec B, Senecal J.
    Arch Ophtalmol Rev Gen Ophtalmol; 1972 Jan; 32(6):457-76. PubMed ID: 4264548
    [No Abstract] [Full Text] [Related]

  • 27. [Cytogenetical investigations on autopsy material (author's transl)].
    Waller H, Waller M.
    Zentralbl Allg Pathol; 1973 Jan; 117(2):138-45. PubMed ID: 4270524
    [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. Results of 538 chromosome studies on patients referred for cytogenetic analysis.
    Mulcahy MT, Jenkyn J.
    Med J Aust; 1972 Dec 09; 2(24):1333-8. PubMed ID: 4265391
    [No Abstract] [Full Text] [Related]

  • 30. [Chromosome aberration and mental retardation].
    Asaka A.
    Shinkei Kenkyu No Shimpo; 1972 Apr 09; 16(2):226-31. PubMed ID: 4260444
    [No Abstract] [Full Text] [Related]

  • 31. [Mosaic 14 trisomy in a female child with multiple abnormalities].
    Rethoré MO, Couturier J, Carpentier S, Ferrand J, Lejeune J.
    Ann Genet; 1975 Mar 09; 18(1):71-4. PubMed ID: 1080041
    [Abstract] [Full Text] [Related]

  • 32. Structural variation in human nitotic chromosomes.
    Leisti J.
    Ann Acad Sci Fenn Biol; 1971 Mar 09; 179():1-69. PubMed ID: 4261167
    [No Abstract] [Full Text] [Related]

  • 33. A cytogenetic survey of 11,680 newborn infants.
    Jacobs PA, Melville M, Ratcliffe S, Keay AJ, Syme J.
    Ann Hum Genet; 1974 May 09; 37(4):359-76. PubMed ID: 4277977
    [No Abstract] [Full Text] [Related]

  • 34. Intrauterine growth in autosomal trisomy syndromes.
    Járai I, Méhes K.
    Acta Paediatr Acad Sci Hung; 1973 May 09; 14(2):113-7. PubMed ID: 4271689
    [No Abstract] [Full Text] [Related]

  • 35. Phenotypic overlapping of autosomal trisomy syndromes and its significance.
    Balakrishnan S, Puri RK, Bhargava I.
    Indian Pediatr; 1971 Jul 09; 8(7):336-41. PubMed ID: 5113591
    [No Abstract] [Full Text] [Related]

  • 36. Double autosomal trisomy (trisomy D+G) with mosaicism.
    Porter IH, Petersen W, Brown CD.
    J Med Genet; 1969 Sep 09; 6(3):347-8. PubMed ID: 4242069
    [No Abstract] [Full Text] [Related]

  • 37. Congenital heart diseases and chromosomal abnormalities. A scientific exhibit.
    Maragos GD, Greene CA.
    Nebr Med J; 1972 Apr 09; 57(4):119-20. PubMed ID: 5060008
    [No Abstract] [Full Text] [Related]

  • 38. Chromosome aberrations in 2159 consecutive newborn babies.
    Sergovich F, Valentine GH, Chen AT, Kinch RA, Smout MS.
    N Engl J Med; 1969 Apr 17; 280(16):851-5. PubMed ID: 4238063
    [No Abstract] [Full Text] [Related]

  • 39. [Ocular findings in chromosome diseases].
    Cagianut B.
    Ophthalmologica; 1968 Apr 17; 155(2):148-66. PubMed ID: 4965902
    [No Abstract] [Full Text] [Related]

  • 40. Prenatal chromosome determination. A study of 219 cases.
    Wahlström J, Bartsch FK, Lundberg J.
    Clin Genet; 1974 Apr 17; 6(3):184-91. PubMed ID: 4279153
    [No Abstract] [Full Text] [Related]


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