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Journal Abstract Search


223 related items for PubMed ID: 4345621

  • 1. A short, retarded child with a deletion of the short arm of chromosome 18 (18p-).
    Parker CE, Donnell GN, Mavalwala J, Hurst N, Derencsenyi A.
    Clin Pediatr (Phila); 1973 Jan; 12(1):42-6. PubMed ID: 4345621
    [No Abstract] [Full Text] [Related]

  • 2. [Deficiency at the short arm of chromosome No. 18 (46, XX, 18p-). A uniform abnormality syndrome].
    Reinwein H, Struwe FE, Bettecken F, Wolf U.
    Monatsschr Kinderheilkd (1902); 1968 Sep; 116(9):511-4. PubMed ID: 5682047
    [No Abstract] [Full Text] [Related]

  • 3. [18p-Syndrome. Deletion of the short arm of chromosome 18].
    Jacobsen P.
    Ugeskr Laeger; 1973 Jan 01; 135(1):17. PubMed ID: 4684842
    [No Abstract] [Full Text] [Related]

  • 4. A case with short arm deletion of chromosome 18 (18p-syndrome).
    Kumagai M, Kikuchi Y, Oishi H, Matsuda E, Kato J.
    Jinrui Idengaku Zasshi; 1973 Jun 01; 18(1):24-36. PubMed ID: 4796358
    [No Abstract] [Full Text] [Related]

  • 5. D/E translocation in a young girl.
    Miller JQ, Selden RF, Meisner LF.
    South Med J; 1970 Apr 01; 63(4):368-70. PubMed ID: 5437582
    [No Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7. [The deletion of the short arm of chromosome 18 (18p- syndrome), apropos of a new observation].
    Gilgenkrantz S, Marchal C, Neimann N.
    Ann Genet; 1968 Mar 01; 11(1):17-21. PubMed ID: 5301751
    [No Abstract] [Full Text] [Related]

  • 8.
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  • 9. [Short-arm deletion of chromosome 18 due to a t(G-;18p+) translocation. Fluorescence study with quinacrine mustard].
    Malpuech G, Raynaud EJ, Belin J, Godeneche P, de Grouchy J.
    Ann Genet; 1971 Sep 01; 14(3):213-8. PubMed ID: 5315468
    [No Abstract] [Full Text] [Related]

  • 10. Immunoglobulin abnormality in a girl with a large chromosome 18.
    Yanagisawa S.
    J Med Genet; 1972 Sep 01; 9(3):360-5. PubMed ID: 4116772
    [No Abstract] [Full Text] [Related]

  • 11. Chromosome 18 abnormalities in a family with a translocation t(18p--, 21p+).
    Jacobsen P, Mikkelsen M.
    J Ment Defic Res; 1968 Jun 01; 12(2):144-61. PubMed ID: 5663940
    [No Abstract] [Full Text] [Related]

  • 12. PARTIAL DELETION OF THE SHORT ARMS OF A CHROMOSOME OF THE 4-5 GROUP (DENVER).
    DYGGVE HV, MIKKELSEN M.
    Arch Dis Child; 1965 Feb 01; 40(209):82-5. PubMed ID: 14259280
    [No Abstract] [Full Text] [Related]

  • 13. A case of the 18p--syndrome.
    Subrt I, Beránková J.
    Humangenetik; 1972 Feb 01; 16(4):359-60. PubMed ID: 4641844
    [No Abstract] [Full Text] [Related]

  • 14. Autosomal deletion syndrome 46,XX,18p-: a new case report with absence of IgA in serum.
    Fischer P, Golob E, Friedrich F, Kunze-Mühl E, Doleschel W, Aichmair H.
    J Med Genet; 1970 Mar 01; 7(1):91-8. PubMed ID: 5480972
    [No Abstract] [Full Text] [Related]

  • 15. [The clinical features of the 18 q-syndrome (author's transl)].
    Feichtinger C, Glatzl J.
    Wien Klin Wochenschr; 1974 Aug 16; 86(15):441-4. PubMed ID: 4605988
    [No Abstract] [Full Text] [Related]

  • 16. A mentally retarded boy with multiple congenital anomalies and aberrant morphology in a no. 18 chromosome.
    Van Kempen C.
    Dev Med Child Neurol; 1967 Oct 16; 9(5):617-24. PubMed ID: 6066027
    [No Abstract] [Full Text] [Related]

  • 17. An extra small metacentric chromosome in a mentally retarded boy.
    Ishmael J, Laurence KM.
    J Med Genet; 1968 Dec 16; 5(4):335-40. PubMed ID: 5713650
    [No Abstract] [Full Text] [Related]

  • 18. Identification of 21r and 22r chromosomes by quinacrine fluorescence.
    Crandall BF, Weber F, Muller HM, Burwell JK.
    Clin Genet; 1972 Dec 16; 3(4):264-70. PubMed ID: 5054320
    [No Abstract] [Full Text] [Related]

  • 19. [The syndrome of the deletion of the short arm of a chromosome 4-5].
    Ricci N, Ventimiglia B, Dallapiccola B, Franceschini F, Preto G.
    Acta Genet Med Gemellol (Roma); 1966 Jan 16; 15(1):36-50. PubMed ID: 5930171
    [No Abstract] [Full Text] [Related]

  • 20. [Chromosome 18 long arm deletion. A case with unusual dermatoglyphics].
    Le Marec B, Lessard M, Renault A, Coutel Y.
    Pediatrie; 1971 Jan 16; 26(7):749-57. PubMed ID: 5118994
    [No Abstract] [Full Text] [Related]


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