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Journal Abstract Search

392 related items for PubMed ID: 5314290

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  • 2. [Partial trisomy C through a familial translocation t(Cq+;Cq-)].
    Lejeune J, Rethoré MO, Berger R, Abonyi D, Dutrillaux B, See G.
    Ann Genet; 1968 Sep; 11(3):171-5. PubMed ID: 5304617
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  • 6. Partial trisomy 9 in the case of familial translocation 8/9 mat.
    Schwanitz G, Schamberger U, Rott HD, Wieczorek V.
    Ann Genet; 1974 Sep; 17(3):163-6. PubMed ID: 4548816
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  • 7. 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
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  • 8. Structural variation in human nitotic chromosomes.
    Leisti J.
    Ann Acad Sci Fenn Biol; 1971 Jun 01; 179():1-69. PubMed ID: 4261167
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  • 10. [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 01; 13(4):217-32. PubMed ID: 5313386
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  • 11. [Partial trisomy 11q;22q (author's transl)].
    Benítez J, Ayuso C, García Aparicio J, Sáez E, Pérez Sotelo A, Bello MJ.
    An Esp Pediatr; 1981 Sep 01; 15(3):293-300. PubMed ID: 7332142
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  • 15. 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
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  • 18. 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 Apr 01; 13(3B):167-86. PubMed ID: 890090
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  • 20. [A case of C-D translocation in a 9 year old boy and his mother].
    Revazov AA, Russkikh VV.
    Tsitologiia; 1966 Apr 01; 8(2):269-76. PubMed ID: 5984073
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