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Journal Abstract Search

97 related items for PubMed ID: 4546343

  • 1. [Ring chromosome 6. Karotype 46, XY, r (6)-45, XY,-6].
    Van den Berghe H, Fryns JP, Cassiman JJ, David G.
    Ann Genet; 1974 Mar; 17(1):29-35. PubMed ID: 4546343
    [No Abstract] [Full Text] [Related]

  • 2. [Ring chromosomes in mosaicism 46, XY, Cr-46, XY].
    Ferrier S, Freund M, Grétillat A.
    Arch Genet (Zur); 1973 Mar; 46(1):1-14. PubMed ID: 4731928
    [No Abstract] [Full Text] [Related]

  • 3. [Study by fluorescence of a trisomy C mosaic, probably 8: 46,XY-47,XY,?8+].
    de Grouchy J, Turleau C, Léonard C.
    Ann Genet; 1971 Mar; 14(1):69-72. PubMed ID: 5314298
    [No Abstract] [Full Text] [Related]

  • 4. Phenotype associated with ring 10 chromosome: report of patient and review of literature.
    Michels VV, Driscoll DJ, Ledbetter DH, Riccardi VM.
    Am J Med Genet; 1981 Mar; 9(3):231-7. PubMed ID: 7025632
    [Abstract] [Full Text] [Related]

  • 5. [Ring chromosome 8 (46,XY, 8 r) in a boy with debility (author's transl)].
    Pfeiffer RA, Lenard HG.
    Klin Padiatr; 1973 May; 185(3):187-91. PubMed ID: 4795572
    [No Abstract] [Full Text] [Related]

  • 6. [C-G translocation: karyotype 46, XY,t(Cq-; Gq+): parents 46, XX and 46, XY].
    Lambotte C, Carlier G, Frederic J, Keutgen J.
    Acta Paediatr Belg; 1971 May; 25(2):119-26. PubMed ID: 5565831
    [No Abstract] [Full Text] [Related]

  • 7. Report of a patient with a ring chromosome 10: mos45,XY,-10/46,XY/46,XY,r(10)(p15.3q26.3).
    Kishi K, Ikeuchi T, Yamamoto K, Tonomura A, Sakurada N, Satoh Y.
    Jinrui Idengaku Zasshi; 1985 Sep; 30(3):233-8. PubMed ID: 3834204
    [No Abstract] [Full Text] [Related]

  • 8. [46,XY-45,X mosaicism and 18p- deletion].
    Giraud F, Hartung M, Mattei JF, Passeron P, Coignet J.
    Ann Genet; 1971 Mar; 14(1):59-62. PubMed ID: 5314297
    [No Abstract] [Full Text] [Related]

  • 9. Ring chromosome 4 : 46,XY, r(4) (p16q35) in a boy.
    Gutkowska A, Krajewska-Walasek M, Wiśniewski L.
    Klin Padiatr; 1985 Mar; 197(4):294-6. PubMed ID: 4046483
    [Abstract] [Full Text] [Related]

  • 10. Abnormalities of human autosomes. I. Ambigous genitalia associated with a translocation 46,XY, t(Cq+;Cq-).
    German J, Simpson JL.
    Birth Defects Orig Artic Ser; 1971 May; 7(6):145-9. PubMed ID: 5173157
    [Abstract] [Full Text] [Related]

  • 11. [Clinical and cytogenetic observations on 2 mosaic C trisomic adults. Individualization of the supernumerary chromosome with the modern denaturation technic: 47, XY, ?8 +].
    Laurent C, Robert JM, Grambert J, Dutrillaux B.
    Lyon Med; 1971 Dec 26; 226(20):827-33. PubMed ID: 5144392
    [No Abstract] [Full Text] [Related]

  • 12. Ring chromosome 4 mosaicism and Potter sequence.
    Fryns JP, Kleczkowska A, Jaeken J, Van den Berghe H.
    Ann Genet; 1988 Dec 26; 31(2):120-2. PubMed ID: 3261147
    [Abstract] [Full Text] [Related]

  • 13. [Morphologic abnormality due to duplication of chromosome 17 (46,XY,17q+) in a newborn infant].
    Fouquette B, Rosenfeld R, Cadotte M.
    Union Med Can; 1974 Aug 26; 103(8):1404-8. PubMed ID: 4849205
    [No Abstract] [Full Text] [Related]

  • 14. A family with a presumptive C-F translocation in five generations.
    Therkelsen AJ, Klinge T, Henningsen K, Mikkelsen M, Schmidt G.
    Ann Genet; 1971 Mar 26; 14(1):13-21. PubMed ID: 5314290
    [No Abstract] [Full Text] [Related]

  • 15. [Ring chromosome 13 and multiple malformations (author's transl)].
    Antich J, Plaza J, Geán E.
    An Esp Pediatr; 1981 Nov 26; 15(5):469-73. PubMed ID: 7332149
    [Abstract] [Full Text] [Related]

  • 16. 46,XY-47,XY,C+ mosaicism in a male infant with multiple anomalies.
    Oikawa K, Kajii T, Shimba H, Sasaki M.
    Ann Genet; 1969 Jun 26; 12(2):102-6. PubMed ID: 5308379
    [No Abstract] [Full Text] [Related]

  • 17. [Trisomy 10 p. Apropos of a case caused by a maternal translocation].
    Stoll C, Willard D.
    Pediatrie; 1980 Jun 26; 35(3):251-5. PubMed ID: 7393692
    [No Abstract] [Full Text] [Related]

  • 18. [Chromosomal mosaicism in the r (15) syndrome].
    Malygina NA, Mutovin GR, Filina NP, Akif'ev AP.
    Genetika; 1980 Jun 26; 16(11):2029-33. PubMed ID: 7193157
    [Abstract] [Full Text] [Related]

  • 19. Isochromosome 21 and other chromosomal abnormalities in a patient with erythroleukaemia.
    Werner-Favre C, Cabrol C, Beris P, Engel E.
    Ann Genet; 1983 Jun 26; 26(4):240-2. PubMed ID: 6607706
    [Abstract] [Full Text] [Related]

  • 20. A ring chromosome (46,XY,13r) occurring in a family with a D-D translocation 13-,14-, t(13q 14q).
    Mikkelsen M, Niebuhr E.
    Ann Genet; 1969 Mar 26; 12(1):51-6. PubMed ID: 5306712
    [No Abstract] [Full Text] [Related]

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