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Journal Abstract Search

185 related items for PubMed ID: 49427

  • 1.
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  • 2. Three non-mongoloid patients of similar phenotype with an extra G-like chromosome.
    Gustavson KH, Hitrec V, Santesson B.
    Clin Genet; 1972; 3(2):135-46. PubMed ID: 5054315
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  • 4. Phenotype of partial trisomy 8 (p21 leads to qter) in two unrelated patients with de novo translocation.
    Sachs ES, van Waveren G.
    J Med Genet; 1981 Jun; 18(3):204-8. PubMed ID: 7241543
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  • 6. [Autosomal chromosome aberrations].
    Serville F, Battin J.
    Bord Med; 1971 May; 4(5):1373-416. PubMed ID: 5105683
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  • 7. [Giemsa-R-banding analysis of the trisomy 9p and report of a new case].
    Rethoré MO, Hoehn H, Rott HD, Couturier J, Dutrillaux B, Lejeune J.
    Humangenetik; 1973 Apr 16; 18(2):129-38. PubMed ID: 4124236
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  • 8. Segregating reciprocal (4;21) (q21;q21) translocation with proposita trisomic for parts of 4q and 21.
    De la Chapelle A, Koivisto M, Schröder J.
    J Med Genet; 1973 Dec 16; 10(4):384-9. PubMed ID: 4129974
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  • 11. [Partial C trisomy through translocation t(Cp-;Gp-)].
    Deminatti M, Maillard E, Gosselin B, Peltier JM, Bulteel MF, Dupuis C.
    Ann Genet; 1969 Mar 16; 12(1):36-45. PubMed ID: 5306710
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  • 12. A case of extra small acrocentric bisatellited chromosome in a non mongoloid child.
    Furbetta M, Rosi G, Biagioni M, Cossu P, Cao A.
    Humangenetik; 1975 Sep 20; 30(3):259-63. PubMed ID: 1184008
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  • 13. Trisomy 22 mosaicism with normal blood chromosomes. Case report with literature review.
    Lessick ML, Szego K, Wong PW.
    Clin Pediatr (Phila); 1988 Sep 20; 27(9):451-4. PubMed ID: 3046809
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  • 14. Familial partial trisomy of the long arm of chromosome 10 (q24-26).
    Moreno-Fuenmayor H, Zackai EH, Mellman WJ, Aronson M.
    Pediatrics; 1975 Nov 20; 56(5):756-61. PubMed ID: 1196732
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  • 15. An (11;21) translocation in four generations with chromosome 11 abnormalities in the offspring. A clinical, cytogenetical, and gene marker study.
    Jacobsen P, Hauge M, Henningsen K, Hobolth N, Mikkelsen M, Philip J.
    Hum Hered; 1973 Nov 20; 23(6):568-85. PubMed ID: 4134631
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  • 16. Phenotype-karyotype correlations in dup(18q): report of a case and review.
    Razavi-Encha F, Raoul O, Lescs MC, Danan C.
    Am J Med Genet; 1985 Jul 20; 21(3):591-5. PubMed ID: 4025391
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  • 17. Partial trisomy 15 in a young girl.
    Mankinen CB, Hold JG, Sears JW.
    Clin Genet; 1976 Jul 20; 10(1):27-32. PubMed ID: 949862
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  • 18. ["Free" 9p trisomy in a male child with severe mental retardation (author's transl)].
    Aller V, Abrisqueta JA, Martín-Lucas MA, de Torres ML, del Mazo J, Pérez-Castillo A.
    An Esp Pediatr; 1979 May 20; 12(5):463-8. PubMed ID: 464416
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