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Journal Abstract Search

150 related items for PubMed ID: 5449945

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  • 3. Identification of 21r and 22r chromosomes by quinacrine fluorescence.
    Crandall BF, Weber F, Muller HM, Burwell JK.
    Clin Genet; 1972; 3(4):264-70. PubMed ID: 5054320
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  • 4. [Pericentric inversion, inv(10), in a mother and aneusomy by recombination, inv(10), rec(10), in her son (author's transl)].
    Dutrillaux B, Laurent C, Robert JM, Lejeune J.
    Cytogenet Cell Genet; 1973; 12(4):245-53. PubMed ID: 4752866
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  • 9. Trisomy 18.
    James AE, Belcourt CL, Atkins L, Janower ML.
    Radiology; 1969 Jan; 92(1):37-43. PubMed ID: 4236175
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  • 10. The 13q-deletion syndrome.
    Allderdice PW, Davis JG, Miller OJ, Klinger HP, Warburton D, Miller DA, Allen FH, Abrams CA, McGilvray E.
    Am J Hum Genet; 1969 Sep; 21(5):499-512. PubMed ID: 5347076
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  • 11. [Ocular manifestations of trisomy 18].
    Ardouin M, Urvoy M, Lautridou A, Le Marec B, Senecal J.
    Arch Ophtalmol Rev Gen Ophtalmol; 1972 Sep; 32(6):457-76. PubMed ID: 4264548
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  • 13. Reciprocal translocation versus centric fusion between two No. 13 chromosomes. A case of 46,XX,-13,+t(13;13)(p12;q13) and a case of 46,XY,-13,+t(13;13)(p12;p12).
    Hsu LY, Kim HJ, Sujansky E, Kousseff B, Hirschhorn K.
    Cytogenet Cell Genet; 1973 Sep; 12(4):235-44. PubMed ID: 4752865
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  • 16. Coloboma and microphthalmos in chromosomal aberrations. Chromosomal aberrations and neural crest cell developmental field.
    Warburg M, Friedrich U.
    Ophthalmic Paediatr Genet; 1987 Jun; 8(2):105-18. PubMed ID: 3309769
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  • 17. Autosomal chromosome aberrations in ophthalmology.
    Francois J.
    Int Ophthalmol Clin; 1968 Jun; 8(4):839-910. PubMed ID: 4244691
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  • 18. Trisomy 13 with a 13q14q translocation.
    Coco R, Penchaszadeh B.
    J Genet Hum; 1975 Mar; 23(1):1-6. PubMed ID: 1165477
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  • 19. Trisomy 13-15.
    James AE, Belcourt CL, Atkins L, Janower ML.
    Radiology; 1969 Jan; 92(1):44-9. PubMed ID: 4302761
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