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Journal Abstract Search

383 related items for PubMed ID: 5097149

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  • 6. A complex mosaic with tdic(13;18) (p11;p11), +13p-, +18p-, r(13) etc. in a male infant. I. Centromere inactivation and dissociation of dicentric chromosome.
    Uehara M, Kida M.
    Jinrui Idengaku Zasshi; 1986 Mar; 31(1):27-35. PubMed ID: 3735756
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  • 7. Trisomy 22 mosaicism with normal blood chromosomes. Case report with literature review.
    Lessick ML, Szego K, Wong PW.
    Clin Pediatr (Phila); 1988 Sep; 27(9):451-4. PubMed ID: 3046809
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  • 9. [Hereditary mosaicism: normal-trisomy D, chromosome fragility and new type of mosaicism with D ringformation in descendents].
    Zdansky R, Rett A, Piperger A.
    Fortschr Med; 1972 Jul 06; 90(19):748-52. PubMed ID: 5073851
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  • 10. [Trisomy 18].
    Berger R.
    Nouv Presse Med; 1972 Mar 11; 1(11):745-8. PubMed ID: 5022253
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  • 12. Trisomy 13 in two infants with cyclops.
    Fujimoto A, Ebbin AJ, Towner JW, Wilson MG.
    J Med Genet; 1973 Sep 11; 10(3):294-6. PubMed ID: 4204339
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  • 14. Chromosome constitution and its bearing on the chromosomal radiosensitivity in man.
    Sasaki MS, Tonomura A, Matsubara S.
    Mutat Res; 1970 Dec 11; 10(6):617-33. PubMed ID: 4253911
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  • 15. Autosomal chromosome aberrations in ophthalmology.
    Francois J.
    Int Ophthalmol Clin; 1968 Dec 11; 8(4):839-910. PubMed ID: 4244691
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  • 18. Genetic heterogeneity of cebocephaly.
    Holmes LB, Driscoll S, Atkins L.
    J Med Genet; 1974 Mar 11; 11(1):35-40. PubMed ID: 4837285
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  • 19. A double aneuploid mosaic: trisomy 13 and XXY.
    Ebbin AJ, Chu Lim R, Towner JW, Wilson MG.
    J Med Genet; 1972 Sep 11; 9(3):365-7. PubMed ID: 5079108
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