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Journal Abstract Search

131 related items for PubMed ID: 5316134

  • 21. [The importance of configurations or papillary lines in the identification of chromosomal diseases].
    Rott HD.
    Folia Clin Int (Barc); 1969 Oct; 19(10):500-6. PubMed ID: 5396731
    [No Abstract] [Full Text] [Related]

  • 22. A case of 48, XXX, +18 double trisomy.
    Imai I, Shimao S, Suzuki Y, Okada T.
    Acta Paediatr Jpn; 1987 Feb; 29(1):178-81. PubMed ID: 3144845
    [No Abstract] [Full Text] [Related]

  • 23. [Cytogenetics in pediatric practice. Experience of 10 years (author's transl)].
    Carnevale A, Blanco B, Frías S, Castillo J, Vázquez V.
    Rev Invest Clin; 1981 Feb; 33(2):175-81. PubMed ID: 7291763
    [No Abstract] [Full Text] [Related]

  • 24. [D trisomy. 2 cases with characteristic phenotype].
    Giovannucci ML, Calabri G, Paoli A.
    Riv Clin Pediatr; 1969 Feb; 82():320-9. PubMed ID: 5405486
    [No Abstract] [Full Text] [Related]

  • 25. [Unusual chromosomal rearrangement. An autosomal telomeric translocation on a multicentury satellited Y (Yqs) chromosome].
    Genest P, Genest FB, Gagnon-Blais D.
    Ann Genet; 1983 Feb; 26(2):86-90. PubMed ID: 6604491
    [Abstract] [Full Text] [Related]

  • 26. [Trisomy syndrome D (47, XY, D+) in a newborn].
    Majlert T, Jaworska M, Stolarska A.
    Pediatr Pol; 1970 Nov; 45(11):1379-82. PubMed ID: 5496174
    [No Abstract] [Full Text] [Related]

  • 27. [Trisomy 18 in 2 newborn infants with rare abnormalities in one of them].
    Bruni L, Castello MA, Crucioli V, Zucco V.
    Riv Ostet Ginecol; 1969 Feb; 24(2):60-73. PubMed ID: 5399531
    [No Abstract] [Full Text] [Related]

  • 28. [3 cases of trisomy 18(trisomy E) found among 10,000 children born alive: typical and atypical forms].
    Raichs A, Tamparillas M, Marco L.
    Sangre (Barc); 1967 Feb; 12(3):313-26. PubMed ID: 5601788
    [No Abstract] [Full Text] [Related]

  • 29. Human chromosome analysis: methodology and applications.
    Larson L.
    Am J Med Technol; 1983 Oct; 49(10):687-98. PubMed ID: 6228140
    [Abstract] [Full Text] [Related]

  • 30. An unbalanced karyotype in a translocation (Cq-,Aq+) pedigree.
    Smith GF, Shear CS, Jalowayski I, Akesson HO.
    J Ment Defic Res; 1969 Jun; 13(2):123-9. PubMed ID: 5794286
    [No Abstract] [Full Text] [Related]

  • 31. Isochromosome 18q in a girl with holoprosencephaly, DiGeorge anomaly, and streak ovaries.
    van Essen AJ, Schoots CJ, van Lingen RA, Mourits MJ, Tuerlings JH, Leegte B.
    Am J Med Genet; 1993 Aug 01; 47(1):85-8. PubMed ID: 8368259
    [Abstract] [Full Text] [Related]

  • 32. Triple-x syndrome accompanied by congenital adrenal hyperplasia: case report.
    Kurtoğlu S, Atabek ME, Akçakuş M, Ozkul Y, Saatçi C.
    Turk J Pediatr; 2004 Aug 01; 46(4):377-9. PubMed ID: 15641277
    [Abstract] [Full Text] [Related]

  • 33. A liveborn case of 49,XXXY, + 18.
    Kardon NB, Berger AL, Elice M, Davis JG, Jenkins EC.
    J Med Genet; 1980 Oct 01; 17(5):389-90. PubMed ID: 7194375
    [Abstract] [Full Text] [Related]

  • 34. [Late prenatal diagnosis of fetal growth retardation: the diagnosis of a case of trisomy 18 (author's transl)].
    Le Marec B, Defawe G, Mention JE, Picard F, Duval JM, Dubois J.
    J Gynecol Obstet Biol Reprod (Paris); 1980 Oct 01; 9(6):655-7. PubMed ID: 7462570
    [Abstract] [Full Text] [Related]

  • 35. [Trisomy 18].
    Otero de Rovner I, Mide de Piterbarg S, Koloditzky D.
    Arch Argent Pediatr; 1969 Oct 01; 67(2):41-50. PubMed ID: 5385768
    [No Abstract] [Full Text] [Related]

  • 36. First report of a patient with a mixoploidy 47,XXX/94,XXXXXX.
    Rodríguez Criado G, Galán Gómez E, Tizzano EF, García Rodríguez E, Gómez de Terreros I.
    Genet Couns; 2007 Oct 01; 18(1):99-104. PubMed ID: 17515305
    [Abstract] [Full Text] [Related]

  • 37. Autoimmunity in a patient with 47,XXX karyotype.
    Michalak DP, Zacur HA, Rock JA, Woodruff JD.
    Obstet Gynecol; 1983 Nov 01; 62(5):667-9. PubMed ID: 6621958
    [Abstract] [Full Text] [Related]

  • 38. [Increased activity of adenine phosphoribosyl transferase in a child trisomic for 16q22.2 to 16qter due to malsegregation of a t(16;21) (q22.2;q22;2)pat (author's transl)].
    Rethoré MO, Lafourcade J, Couturier J, Harpey JP, Hamet M, Engler R, Alcindor LG, Lejeune J.
    Ann Genet; 1982 Nov 01; 25(1):36-42. PubMed ID: 6979298
    [Abstract] [Full Text] [Related]

  • 39. Edwards' syndrome with double trisomy (possible tetrasomy) of the E group chromosomes (17-18).
    Korányi G, László J.
    Acta Paediatr Acad Sci Hung; 1969 Nov 01; 10(2):167-75. PubMed ID: 5367786
    [No Abstract] [Full Text] [Related]

  • 40. [XYY syndrome and trisomy 21 (48, XYY, 21+). A phenotype showing a combined autosomal and gonosomal chromosome aberrations].
    Murken JD, Lippoldmüller E, Spiess H.
    Monatsschr Kinderheilkd (1902); 1972 Nov 01; 120(11):469-71. PubMed ID: 4264493
    [No Abstract] [Full Text] [Related]

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