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Journal Abstract Search

147 related items for PubMed ID: 7695369

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  • 3. Dermatoglyphic peculiarities in Down's syndrome detection of mosaicism and balanced translocation carriers.
    Rodewald A, Zang KD, Zankl H, Zankl M.
    Hum Genet Suppl; 1981; 2():41-56. PubMed ID: 6218140
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  • 4. [Cytogenetic findings in patients with Down's syndrome].
    Cortés F, Alliende M, Curotto B.
    Rev Chil Pediatr; 1990; 61(6):313-6. PubMed ID: 2152215
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  • 6. Recurrent trisomy 21 in a couple with a child presenting trisomy 21 mosaicism and maternal uniparental disomy for chromosome 21 in the euploid cell line.
    Bruyère H, Rupps R, Kuchinka BD, Friedman JM, Robinson WP.
    Am J Med Genet; 2000 Sep 04; 94(1):35-41. PubMed ID: 10982480
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  • 9. Trisomy 21 mosaicism in a woman with two children with trisomy 21 Down's syndrome.
    Kaffe S, Hsu LY, Hirschhorn K.
    J Med Genet; 1974 Dec 04; 11(4):378-9. PubMed ID: 4140911
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  • 10. Down's syndrome in Western Australia: cytogenetics and incidence.
    Mulcahy MT.
    Hum Genet; 1979 Apr 17; 48(1):67-72. PubMed ID: 156692
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  • 17. Down's syndrome transmitted through maternal mosaicism.
    Aarskog D.
    Acta Paediatr Scand; 1969 Nov 17; 58(6):609-14. PubMed ID: 4244880
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  • 19. [Complete Down's syndrome in a boy, formed by chromosomic mosaicism 46-XY isochromosome 21 and 47-XY, trisomy 21 with mosaicism of the mother 46-XX and 47-XX, trisomy 21)].
    Raichs A, Tamparillas M.
    Sangre (Barc); 1967 Nov 17; 12(1):71-80. PubMed ID: 4235850
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