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Journal Abstract Search

459 related items for PubMed ID: 4272425

  • 1.
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  • 3. Double aneuploidy in three Egyptian patients: Down-Turner and Down-Klinefelter syndromes.
    Zaki MS, Kamel AA, El-Ruby M.
    Genet Couns; 2005; 16(4):393-402. PubMed ID: 16440882
    [Abstract] [Full Text] [Related]

  • 4. Turner's syndrome and Duchenne muscular dystrophy in a girl with an X; autosome translocation.
    Bjerglund Nielsen L, Nielsen IM.
    Ann Genet; 1984; 27(3):173-7. PubMed ID: 6334482
    [Abstract] [Full Text] [Related]

  • 5. [Association of a case of Turner's syndrome with familial t(Cq-; Gp+)].
    Laurent C, Bonnet P, Farouz S, Longin B.
    Ann Genet; 1970 Mar; 13(1):61-6. PubMed ID: 5310107
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  • 6. [Double aneuploidy: 46,XX-45,XO-47,XX,G+. Case report].
    Grosse KP, Hopfengärtner F, Schwanitz G.
    Humangenetik; 1971 Mar; 13(4):333-7. PubMed ID: 4257570
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  • 8. Mosaic double aneuploidy of X and G chromosomes.
    Osborne RA, Hennigar GR, Barnett CD.
    Am J Ment Defic; 1975 May; 79(6):644-7. PubMed ID: 125038
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  • 9. [A report of 2 cases of Turner's syndrome with a ring X chromosome].
    Migliori MV, Bartolotta E, Maurizi M, Bonazzi P, Cardinale G, Manunza V.
    Minerva Pediatr; 1991 Sep; 43(9):605-9. PubMed ID: 1758399
    [Abstract] [Full Text] [Related]

  • 10. [Duplication of an X chromosome in a case of Turner's syndrome (45,X-46,XXp+)].
    Emerit I, German J, Crippa LP, Sureau C.
    Ann Genet; 1970 Dec; 13(4):245-8. PubMed ID: 5313888
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  • 11. [Chromosomal determination of pathological personality development in man].
    Firko M, Matuszewicz T, Trembla K.
    Psychiatr Pol; 1971 Dec; 5(3):317-24. PubMed ID: 4256510
    [No Abstract] [Full Text] [Related]

  • 12. G-11 staining in Turner's syndrome with mos 45,X/46,X,r(?).
    de Almeida JC, Llerena JC, Molina Gomes D, Rita Martins R, Jung M, Reis DF, Cunha AG.
    Ann Genet; 1985 Dec; 28(1):37-41. PubMed ID: 2409888
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  • 13. Autosomal/heterosomal mixoploids: a report on two patients, a female with a 45, Z/47,XX plus 21 and a male with A 45,X/47,XY, plus 21 chromosome constitution.
    Hustinx TW, Haar BG, Scheres JM, Rutten FJ.
    Ann Genet; 1974 Dec; 17(4):225-34. PubMed ID: 4281287
    [No Abstract] [Full Text] [Related]

  • 14. Down's/Turner's mosaicism. Double aneuploidy as a rare cause of missed prenatal diagnosis of chromosomal abnormality.
    MacFaul R, Turner T, Mason MK.
    Arch Dis Child; 1981 Dec; 56(12):962-3. PubMed ID: 6460476
    [Abstract] [Full Text] [Related]

  • 15. [A case of Turner's syndrome in 45,X/46,XXp- mosaicism associated with colour-blindness (author's transl)].
    Ferrier S, Crippa L, Cabrol C, Pescia G.
    J Genet Hum; 1976 Jun; 24(2):95-112. PubMed ID: 1085812
    [Abstract] [Full Text] [Related]

  • 16. Non-fluorescent Y-chromosome.
    Bühler EM, Bühler UK, Tsuchimoto T, Stalder GR.
    Helv Paediatr Acta; 1974 Nov; 29(5):447-56. PubMed ID: 4141700
    [No Abstract] [Full Text] [Related]

  • 17. [Y chromosome structural abnormalities and Turner's syndrome].
    Ravel C, Siffroi JP.
    Gynecol Obstet Fertil; 2009 Jun; 37(6):511-8. PubMed ID: 19464936
    [Abstract] [Full Text] [Related]

  • 18. [45,X/ 46,XX/ 46,XY Mosaic with female phenotype].
    Moreau N, Rochet Y, Peyramond C, Raymond D.
    Bull Assoc Anat (Nancy); 1976 Dec; 60(171):757-67. PubMed ID: 1030251
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  • 19. Ring chromosome 21 in phenotypically apparently normal persons: report of two families from Switzerland and Italy.
    Schmid W, Tenconi R, Baccichetti C, Caufin D, Schinzel A.
    Am J Med Genet; 1983 Nov; 16(3):323-9. PubMed ID: 6228144
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  • 20. A dicentric Y chromosome without evidence of sex chromosomal mosaicism, 46,XYqdic, in a patient with features of Turner's syndrome.
    Armendares S, Buentello L, Salamanca F, Cantu-Garza JM.
    J Med Genet; 1972 Mar; 9(1):96-100. PubMed ID: 5063516
    [No Abstract] [Full Text] [Related]

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