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Journal Abstract Search

132 related items for PubMed ID: 571896

  • 1. Familial Y/22 translocation in a woman.
    de Chieri PR.
    J Genet Hum; 1978 Dec; 26(4):297-301. PubMed ID: 571896
    [Abstract] [Full Text] [Related]

  • 2. [Familial translocation 22/Y and partial autosomal trisomy in a young girl].
    Kessel E, Pfeiffer RA, Welling P.
    J Genet Hum; 1979 Mar; 27(1):45-51. PubMed ID: 573310
    [Abstract] [Full Text] [Related]

  • 3. [Reciprocal translocation at the origin of a Robertsonian translocation 15;22 by the loss of a metacentric chromosome. Genetic counseling].
    Pison H, Mattei MG, Jalbert H, Sele B, Leroux D, Augusseau S, Jalbert P.
    J Genet Hum; 1984 Dec; 32(5):363-8. PubMed ID: 6527132
    [Abstract] [Full Text] [Related]

  • 4. Ring chromosome 21 in a normal female.
    Kleczkowska A, Fryns JP.
    Ann Genet; 1984 Dec; 27(2):126-8. PubMed ID: 6331791
    [Abstract] [Full Text] [Related]

  • 5. E trisomy phenotype associated with small metacentric chromosome and a familial Y-22 translocation.
    Dumars KW, Fialko G, Larson E.
    Birth Defects Orig Artic Ser; 1976 Dec; 12(5):97-104. PubMed ID: 953249
    [Abstract] [Full Text] [Related]

  • 6. [Translocation (X; Y) and genetic counseling].
    Mugneret F, Sidaner I, Nivelon-Chevallier A, Koening M, Parise F, Turc-Carel C.
    J Genet Hum; 1988 Jan; 36(1-2):93-7. PubMed ID: 3379384
    [Abstract] [Full Text] [Related]

  • 7.
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  • 8. Translocation 46,X,t(Y;14)(q122;q111) in a case of sterility in the male.
    Petit P, Unglik A, Fryns JP.
    Ann Genet; 1982 Jan; 25(1):63-4. PubMed ID: 6979304
    [No Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
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  • 10. Familial Y-autosome translocation in two unrelated girls.
    Funderburk SJ, Klisak I, Sparkes RS, Carrel RE.
    Ann Genet; 1982 Jan; 25(2):119-22. PubMed ID: 6984628
    [Abstract] [Full Text] [Related]

  • 11. Case of (Y;1) familial translocation.
    Teyssier M, Rafat A, Pugeat M.
    Am J Med Genet; 1993 May 15; 46(3):339-40. PubMed ID: 8488881
    [Abstract] [Full Text] [Related]

  • 12. Prenatal diagnosis of a satellited non-acrocentric chromosome derived from a maternal translocation (10;13)(p13;p12) and review of literature.
    Faivre L, Morichon-Delvallez N, Viot G, Larget-Piet A, Narcy F, Turleau C, Pinson MP, Dumez Y, Munnich A, Vekemans M.
    Prenat Diagn; 1999 Mar 15; 19(3):282-6. PubMed ID: 10210132
    [Abstract] [Full Text] [Related]

  • 13. X-inactivation pattern in three cases of X/autosome translocation.
    Zabel BU, Baumann WA, Pirntke W, Gerhard-Ratschow K.
    Am J Med Genet; 1978 Mar 15; 1(3):309-17. PubMed ID: 677170
    [Abstract] [Full Text] [Related]

  • 14. Prenatal diagnosis of a de novo Y/22 translocation.
    Verjaal M, Treffers PE, Nagal Y, Leschot NJ.
    J Med Genet; 1978 Dec 15; 15(6):475-9. PubMed ID: 570605
    [Abstract] [Full Text] [Related]

  • 15. [Maternal translocation t (1; 8; 15) and trisomy 8 qter in her daughter. Genetic counseling].
    Ballesta F, Fernández E, Milá M.
    J Genet Hum; 1980 Sep 15; 28(3):361-6. PubMed ID: 7463035
    [No Abstract] [Full Text] [Related]

  • 16. [Numerical and structural aberrations of human Y chromosome].
    Parcheta B.
    Pol Tyg Lek; 1980 Apr 14; 35(15):543-6. PubMed ID: 6995959
    [No Abstract] [Full Text] [Related]

  • 17. Trisomy 11q(q21 leads to qter).
    Bader PI, Jansch M, Hoffman D, Palmer CG, Gerber H, Taylor G.
    Birth Defects Orig Artic Ser; 1978 Apr 14; 14(6C):383-92. PubMed ID: 728594
    [No Abstract] [Full Text] [Related]

  • 18. Cytogenetic polymorphism or Y/15 translocation in a black male with ambiguous genitalia.
    Verma RS, Dosik H, Jhaveri RC, Warman J.
    J Genet Hum; 1978 Dec 14; 26(4):405-9. PubMed ID: 752070
    [Abstract] [Full Text] [Related]

  • 19. Molecular analysis of a complex chromosomal rearrangement and a review of familial cases.
    Batista DA, Pai GS, Stetten G.
    Am J Med Genet; 1994 Nov 15; 53(3):255-63. PubMed ID: 7856662
    [Abstract] [Full Text] [Related]

  • 20. Ring chromosome 21 in the mother and 21/21 translocation in the fetus: karyotype: 45,XX,-21,-21,+t(21;21)(p11;q11).
    Fryns JP, Kleczkowska A.
    Ann Genet; 1987 Nov 15; 30(2):109-10. PubMed ID: 3499841
    [Abstract] [Full Text] [Related]

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