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Journal Abstract Search

149 related items for PubMed ID: 5476829

  • 1. [Turner's phenotype syndrome (Noonan's syndrome)].
    Kobielowa Z, Mazurek A, Miezyński W, Sokolowski J.
    Endokrynol Pol; 1970; 21(5):505-15. PubMed ID: 5476829
    [No Abstract] [Full Text] [Related]

  • 2. [Dermatoglyphics in Noonan's syndrome (author's transl)].
    Rott HD, Schwanitz G, Reither M.
    Acta Genet Med Gemellol (Roma); 1975; 24(1-2):63-7. PubMed ID: 1224924
    [Abstract] [Full Text] [Related]

  • 3. [A case of Noonan's syndrome].
    Mozziconacci P, Attal C, Gorin R, Hayem F, Combourieu M, Suied B.
    Ann Pediatr (Paris); 1970 Mar 02; 17(3):220-6. PubMed ID: 5440169
    [No Abstract] [Full Text] [Related]

  • 4. Cardiovascular malformations in Turner's and Noonan's syndrome.
    Van der Hauwaert LG, Fryns JP, Dumoulin M, Logghe N.
    Br Heart J; 1978 May 02; 40(5):500-9. PubMed ID: 656215
    [Abstract] [Full Text] [Related]

  • 5. [The karyotype-phenotype relationship in Turner's syndrome].
    Degenhardt KH.
    Med Welt; 1976 Jan 23; 27(4):136-41. PubMed ID: 1250124
    [No Abstract] [Full Text] [Related]

  • 6. [Hypertrophic cardiomyopathy associated with Noonan's syndrome and membranous aortic subvalvular stenosis associated with Turner's syndrome. Report of 2 clinical cases].
    Perrotta Scaravilli E, Pontillo D, Pennacchia F, Boccanelli A, Greco C, Lo Schiavo P.
    G Ital Cardiol; 1987 Sep 23; 17(9):800-6. PubMed ID: 3692082
    [Abstract] [Full Text] [Related]

  • 7. Turner's phenotype in the male.
    Ferrier PE, Ferrier SA.
    Pediatrics; 1967 Oct 23; 40(4):575-85. PubMed ID: 6051057
    [No Abstract] [Full Text] [Related]

  • 8. [Noonan's syndrome. Genetic and cardiological study of 2 cases].
    Saint-Rome G, Davignon A, Kratz C.
    Union Med Can; 1970 Sep 23; 99(9):1602-12. PubMed ID: 5005748
    [No Abstract] [Full Text] [Related]

  • 9. [Turner's phenotype and diagnosis of Noonan's syndrome].
    Latini G, Berardi R.
    Pediatr Med Chir; 1982 Sep 23; 4(5):535-8. PubMed ID: 6927352
    [Abstract] [Full Text] [Related]

  • 10. [Palmar and plantar dermatoglyphics in Turner's syndrome].
    Gebala A, Dobrzańska A, Grzeszyk C.
    Pediatr Pol; 1970 Mar 23; 45(3):275-84. PubMed ID: 5441588
    [No Abstract] [Full Text] [Related]

  • 11. Noonan's syndrome (XX and XY Turner phenotype) in three generations of a family.
    Baird PA, De Jong BP.
    J Pediatr; 1972 Jan 23; 80(1):110-4. PubMed ID: 5016336
    [No Abstract] [Full Text] [Related]

  • 12. Turner syndrome and Noonan's syndrome.
    Summitt RL.
    J Pediatr; 1969 Jan 23; 74(1):155-6. PubMed ID: 5782821
    [No Abstract] [Full Text] [Related]

  • 13. [3 recent cases of Noonan's syndrome].
    Vellieux F, Saint-Jacques I, Loubry P, Joly T, Boissière H.
    Sem Hop; 1978 Mar 23; 54(5-8):335-43. PubMed ID: 211629
    [Abstract] [Full Text] [Related]

  • 14. Turner's syndrome in one of monozygotic twins with mosaicism.
    Potter AM, Taitz LS.
    Acta Paediatr Scand; 1972 Jul 23; 61(4):473-6. PubMed ID: 5041395
    [No Abstract] [Full Text] [Related]

  • 15. A double chromosomal aberration of the 47, XX, 21+-47, XXp-q-, 21+ type in a girl with features of Down's and Turner's syndromes.
    Mikel'saar AV, Blyumina MG, Kuznetsova LI, Mikel'saar RV, Lur'e IV.
    Sov Genet; 1971 May 23; 7(5):675-9. PubMed ID: 4272425
    [No Abstract] [Full Text] [Related]

  • 16. [Masculine Turner's syndrome].
    Kiss I, Rath F.
    Arch Kinderheilkd; 1970 Mar 23; 180(3):299-308. PubMed ID: 5521978
    [No Abstract] [Full Text] [Related]

  • 17. [Translocation D-D and Turner's syndrome. Considerations on a rare association of chromosome pathology].
    Giovannucci ML, Pierro U, Cordelli F, Paoli A.
    Haematologica; 1969 Mar 23; 54(11):813-26. PubMed ID: 4993250
    [No Abstract] [Full Text] [Related]

  • 18. [Electroencephalographic study of Turner's syndrome].
    Poenaru S, Stanesco V, Poenaru L, Stoian D.
    Acta Neurol Belg; 1970 Mar 23; 70(5):509-22. PubMed ID: 4996762
    [No Abstract] [Full Text] [Related]

  • 19.
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    [No Abstract] [Full Text] [Related]

  • 20. Turner's syndrome: cytogenetic study of a patient included in the initial report of Turner.
    Sparkes RS, Kolodny S.
    J Clin Endocrinol Metab; 1966 May 23; 26(5):577-9. PubMed ID: 5938373
    [No Abstract] [Full Text] [Related]

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