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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

409 related items for PubMed ID: 4731928

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2. Structural variation in human nitotic chromosomes.
    Leisti J.
    Ann Acad Sci Fenn Biol; 1971; 179():1-69. PubMed ID: 4261167
    [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. 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; 12(2):102-6. PubMed ID: 5308379
    [No Abstract] [Full Text] [Related]

  • 5. 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]

  • 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 Dec; 25(2):119-26. PubMed ID: 5565831
    [No Abstract] [Full Text] [Related]

  • 7. [4 cases of trisomy for the short arm of chromosome 9. Individualization of a new morbid entity].
    Rethoré MO, Larget-Piet L, Abonyi D, Boeswillwald M, Berger R, Carpentier S, Cruveiller J, Dutrillau B, Lafourcade J, Penneau M, Lejeune J.
    Ann Genet; 1970 Dec; 13(4):217-32. PubMed ID: 5313386
    [No Abstract] [Full Text] [Related]

  • 8. Familial translocation between chromosomes of groups C and D (46, T(Cq-;Dq+).
    Tal'vik TA, Mikel'saar AV, Mikel'saar RV.
    Sov Genet; 1974 Jun 01; 8(5):651-7. PubMed ID: 4413436
    [No Abstract] [Full Text] [Related]

  • 9. [46,XY-45,X mosaicism and 18p- deletion].
    Giraud F, Hartung M, Mattei JF, Passeron P, Coignet J.
    Ann Genet; 1971 Mar 01; 14(1):59-62. PubMed ID: 5314297
    [No Abstract] [Full Text] [Related]

  • 10. Duplication 11 (q21 to 23 leads to qter) syndrome.
    Francke U, Weber F, Sparkes RS, Mattson PD, Mann J.
    Birth Defects Orig Artic Ser; 1977 Mar 01; 13(3B):167-86. PubMed ID: 890090
    [No Abstract] [Full Text] [Related]

  • 11. Duplication 8q syndrome due to familial chromosome ins(10;8)(q21;q212q22).
    Bowen P, Fitzgerald PH, Gardner RJ, Biederman B, Veale AM.
    Am J Med Genet; 1983 Apr 01; 14(4):635-46. PubMed ID: 6846399
    [Abstract] [Full Text] [Related]

  • 12. Mosaic 46, XY/47,XY, + der(18)t(Y;18)(q11.22;q11.2) karyotype, moderate mental retardation and non-specific dysmorphism.
    Fryns JP, Kleczkowska A, Van Den Berghe H.
    Genet Couns; 1990 Apr 01; 1(2):173-7. PubMed ID: 2081001
    [No Abstract] [Full Text] [Related]

  • 13. 18q- and 18q+ mosaicism in a mentally retarded boy.
    Ausems MG, Bhola SL, Post-Blok CA, Hennekam RC, de France HF.
    Am J Med Genet; 1994 Nov 15; 53(3):296-9. PubMed ID: 7856666
    [Abstract] [Full Text] [Related]

  • 14. Mosaic supernumerary small ring chromosome.
    Fryns JP, van Herck G, van den Berghe H.
    J Genet Hum; 1981 Jun 15; 29(2):151-4. PubMed ID: 7328409
    [No Abstract] [Full Text] [Related]

  • 15. [2:12 (p25;q21) translocation classed at first as 2/X].
    Pasquali F, Zuffardi O, Zamboni G, Bernardi F.
    Ann Genet; 1975 Mar 15; 18(1):64-6. PubMed ID: 50045
    [Abstract] [Full Text] [Related]

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