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Journal Abstract Search

130 related items for PubMed ID: 3601789

  • 1. [A case of a girl with a ring chromosome 18 in the karyotype].
    Midro AT, Czerwińska-Ciechan K, Wiśniewski L, Sawicka A, Marcinkiewicz D.
    Pol Tyg Lek; 1987 Mar 02; 42(9):260-3. PubMed ID: 3601789
    [No Abstract] [Full Text] [Related]

  • 2. [Ring chromosome 22. Description of a new case (1)].
    Gil Benso R, López Ginés C, Gregori Romero M, Galán Sánchez F, Pellín Pérez A.
    An Esp Pediatr; 1991 Jul 02; 35(1):62-4. PubMed ID: 1772175
    [No Abstract] [Full Text] [Related]

  • 3. Transmission of ring chromosome 18 46,XX/46,XX,r(18) mosaicism in a mother and ring chromosome 18 syndrome in her son.
    Fryns JP, Kleczkowska A, Smeets E, Van Den Berghe H.
    Ann Genet; 1992 Jul 02; 35(2):121-3. PubMed ID: 1524410
    [Abstract] [Full Text] [Related]

  • 4. Ring chromosome 22: a case report.
    Severien C, Felix S, Bartholomé K.
    Klin Padiatr; 1991 Jul 02; 203(6):467-9. PubMed ID: 1721941
    [Abstract] [Full Text] [Related]

  • 5. [Syndrome of congenital anomalies in a girl with karyotype 47,XXX].
    Kańska B, Kleczkowska A, Knaus A, Sokolowski J, Stapińska J.
    Pediatr Pol; 1971 Jan 02; 46(1):81-5. PubMed ID: 5545829
    [No Abstract] [Full Text] [Related]

  • 6. Ring chromosome 21. Observation in a female infant.
    Carlo Stella N, Barberi I, Corrado F, Triolo O.
    Ann Genet; 1984 Jan 02; 27(4):249-51. PubMed ID: 6335374
    [Abstract] [Full Text] [Related]

  • 7. [Fluorescence in situ hybridization in 6 patients with alterations of chromosome 18 and in 7 with marker chromosomes].
    Esmer MC, Carnevale A, Gómez L, del Castillo V, Frías S.
    Rev Invest Clin; 1996 Jan 02; 48(1):27-33. PubMed ID: 8815483
    [Abstract] [Full Text] [Related]

  • 8. Brief clinical report: ring-11 chromosome: phenotype-karyotype correlation with deletions of 11q.
    Cousineau AJ, Higgins JV, Scott-Emuakpor AB, Mody G.
    Am J Med Genet; 1983 Jan 02; 14(1):29-35. PubMed ID: 6829609
    [Abstract] [Full Text] [Related]

  • 9. [Ring chromosome 4 in twins].
    Giuffrè L, Cammarata M, Corsello G, Benigno V, Graziano L, Roccella F, Balsamo V.
    Pediatr Med Chir; 1987 Jan 02; 9(3):349-50. PubMed ID: 3671134
    [Abstract] [Full Text] [Related]

  • 10. Ring chromosome 5 associated with severe growth retardation as the sole major physical abnormality.
    Migliori MV, Cherubini V, Bartolotta E, Pettinari A, Pecora R.
    Am J Med Genet; 1994 Jan 01; 49(1):108-10. PubMed ID: 8172236
    [Abstract] [Full Text] [Related]

  • 11. [A new case of a ring shaped chromosome 18 (18 r)].
    Petit P, Poncelet R.
    Ann Genet; 1967 Sep 01; 10(3):134-7. PubMed ID: 5300397
    [No Abstract] [Full Text] [Related]

  • 12. [Ring chromosome 13 (type I) 45,XY,-13/46, XY,r(13)(p11:q34)].
    Díaz-Cardama Sousa I, Mora Gandarillas I, Vázquez Rodríguez M, Viso Lorenzo A, Alonso Villa MJ, Fernández Toral J.
    An Esp Pediatr; 1990 Jun 01; 32(6):556-8. PubMed ID: 2221637
    [No Abstract] [Full Text] [Related]

  • 13. [Ring chromosome 18].
    Andersen UM.
    Ugeskr Laeger; 1992 Nov 09; 154(46):3250-1. PubMed ID: 1462429
    [Abstract] [Full Text] [Related]

  • 14. [A case of translocation t(Cp-; Bp+)].
    Ricci N, Ventimiglia B, Dallapiccola B, Preto G.
    Ann Genet; 1967 Jun 09; 10(2):82-5. PubMed ID: 5298977
    [No Abstract] [Full Text] [Related]

  • 15. [Ring chromosome 10: 46,XX,r(10)(p15q26)].
    Serville F, Briault R, Taillemite JL, Despoisse S, Cotoni P, Broustet A.
    Ann Genet; 1982 Jun 09; 25(3):168-71. PubMed ID: 6982669
    [Abstract] [Full Text] [Related]

  • 16. [Multiple abnormalities in a girl with a 46, XY,17q+ karyotype].
    Engel W, Reinwein H, Bombel D, Ritter H, Wolf U.
    Humangenetik; 1968 Jun 09; 6(4):311-25. PubMed ID: 5713617
    [No Abstract] [Full Text] [Related]

  • 17. [Ring chromosome 9].
    Kontiokari T, Borgström GH, Ritanen-Mohammed UM.
    Duodecim; 1995 Jun 09; 111(5):439-41. PubMed ID: 8674446
    [No Abstract] [Full Text] [Related]

  • 18. [Anomaly of chromosomic structure (46,XX,17q+) in a polymalformed child].
    Walbaum R, Dupuis C, Dehaene P, Delmas-Marsalet Y.
    Ann Genet; 1968 Mar 09; 11(1):53-5. PubMed ID: 5301757
    [No Abstract] [Full Text] [Related]

  • 19. [An observation of ring chromosome 18 (18r)].
    De Grouchy J, Herrault A, Cohen-Solal J.
    Ann Genet; 1968 Mar 09; 11(1):33-8. PubMed ID: 5301753
    [No Abstract] [Full Text] [Related]

  • 20. Boy with celiac disease, malformations, and ring chromosome 13 with deletion 13q32-->qter.
    Talvik I, Ounap K, Bartsch O, Ilus T, Uibo O, Talvik T.
    Am J Med Genet; 2000 Aug 28; 93(5):399-402. PubMed ID: 10951464
    [Abstract] [Full Text] [Related]

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