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Journal Abstract Search


148 related items for PubMed ID: 4139265

  • 1. 48,XXX, plus 18 double trisomy.
    Madahar DP, Dosik H, Wexler I.
    J Med Genet; 1974 Sep; 11(3):309-11. PubMed ID: 4139265
    [Abstract] [Full Text] [Related]

  • 2. 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]

  • 3. An infant with double trisomy (48,XXX, + 18).
    Jaruratanasirikul S, Jinorose U.
    Am J Med Genet; 1994 Jan 15; 49(2):207-10. PubMed ID: 8116670
    [Abstract] [Full Text] [Related]

  • 4. Clinical and postmortem findings of two cases with karyotype: 48, XXX, +18.
    Sonoda T, Ohdo S, Madokoro H, Akimoto K, Ohba K.
    Acta Paediatr Jpn; 1987 Feb 15; 29(1):173-7. PubMed ID: 3144844
    [No Abstract] [Full Text] [Related]

  • 5. 49,XXYY, +18 in a liveborn male.
    Webb GC, Krumins EJ, Leversha MA, Ford GW.
    J Med Genet; 1984 Jun 15; 21(3):232. PubMed ID: 6748025
    [No Abstract] [Full Text] [Related]

  • 6. Double trisomy 48,XXX,+ 18 in a newborn.
    Rosenfeld W, Verma RS, Jhaveri RC, Salazar D, Dosik H.
    Am J Med Genet; 1981 Jun 15; 8(1):67-71. PubMed ID: 7246607
    [Abstract] [Full Text] [Related]

  • 7. A double aneuploid mosaic: trisomy 13 and XXY.
    Ebbin AJ, Chu Lim R, Towner JW, Wilson MG.
    J Med Genet; 1972 Sep 15; 9(3):365-7. PubMed ID: 5079108
    [No Abstract] [Full Text] [Related]

  • 8. [Autoradiographic studies on DNA-replication of human mitotic chromosomes].
    Abe T.
    Jinrui Idengaku Zasshi; 1969 Sep 15; 14(2):107-39. PubMed ID: 4244062
    [No Abstract] [Full Text] [Related]

  • 9. [A case of double trisomy: 48,XXX,18+].
    Emberger JM, Sarran R, Balzing P.
    Ann Genet; 1971 Dec 15; 14(4):301-3. PubMed ID: 5316134
    [No Abstract] [Full Text] [Related]

  • 10. A liveborn case of 49,XXXY, + 18.
    Kardon NB, Berger AL, Elice M, Davis JG, Jenkins EC.
    J Med Genet; 1980 Oct 15; 17(5):389-90. PubMed ID: 7194375
    [Abstract] [Full Text] [Related]

  • 11. A case of double trisomy in a liveborn infant: 48, XXY, "13.
    Malhes JB, Moore CM, Gershank JJ.
    Clin Genet; 1977 Feb 15; 11(2):147-50. PubMed ID: 837565
    [Abstract] [Full Text] [Related]

  • 12. [Trisomy 18 and 47,XXX syndrome in the same sibship].
    Lejeune J, Abonyi D, Berger R, Gautier M, Rethoré MO.
    Ann Genet; 1969 Mar 15; 12(1):59-61. PubMed ID: 5306714
    [No Abstract] [Full Text] [Related]

  • 13. Trisomy of the short arm of chromosome 17.
    Latta E, Hoo JJ.
    Humangenetik; 1974 Mar 15; 23(3):213-7. PubMed ID: 4135958
    [No Abstract] [Full Text] [Related]

  • 14. A child with double trisomy: 48,XYY,+18.
    Felding I, Kristoffersson U.
    Hereditas; 1981 Mar 15; 95(1):169-71. PubMed ID: 7333871
    [No Abstract] [Full Text] [Related]

  • 15. [Double and single aneuploidy 48-E+, XXX-47-E+, XX in Edward's syndrome].
    Waller H, Waller M, Weigel W.
    Dtsch Gesundheitsw; 1969 Jun 19; 24(25):1191-4. PubMed ID: 5376171
    [No Abstract] [Full Text] [Related]

  • 16. Trisomy D-trisomy E mosaicism in an infant male.
    Warren RJ, Keith JI.
    J Med Genet; 1971 Sep 19; 8(3):384-6. PubMed ID: 5097149
    [No Abstract] [Full Text] [Related]

  • 17. Trisomy 18: Edward's syndrome (a case report of 3 cases).
    Bharucha BA, Agarwal UM, Savliwala AS, Kolluri R, Kumta NB.
    J Postgrad Med; 1983 Apr 19; 29(2):129-32. PubMed ID: 6631764
    [No Abstract] [Full Text] [Related]

  • 18. Case report of a 22-week fetus with 47,XXX karyotype and multiple lower mesodermal defects.
    Hoang MP, Wilson KS, Schneider NR, Timmons CF.
    Pediatr Dev Pathol; 1999 Apr 19; 2(1):58-61. PubMed ID: 9841707
    [Abstract] [Full Text] [Related]

  • 19. Trisomy 12p due to familial t(12p-,6q plus) translocation.
    Fryns JP, Van Den Berghe H.
    Humangenetik; 1974 Apr 19; 24(3):247-52. PubMed ID: 4140836
    [No Abstract] [Full Text] [Related]

  • 20. [Apropos of trisomy 18 - a study of 4 observations].
    Gilgenkrantz S, Sapelier J, Thiriet M, Kahn C, Pierson M.
    Ann Genet; 1967 Mar 19; 10(1):32-8. PubMed ID: 5300124
    [No Abstract] [Full Text] [Related]


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