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Journal Abstract Search

275 related items for PubMed ID: 5205520

  • 21. Diagnosis of tetrasomy 18p using in situ hybridization of a DNA probe to metaphase chromosomes.
    Park VM, Gustashaw KM, Bilenker RM, Golden WL.
    Am J Med Genet; 1991 Nov 01; 41(2):180-3. PubMed ID: 1785630
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  • 23. [A case of C-D translocation in a 9 year old boy and his mother].
    Revazov AA, Russkikh VV.
    Tsitologiia; 1966 Nov 01; 8(2):269-76. PubMed ID: 5984073
    [No Abstract] [Full Text] [Related]

  • 24. Interstitial deletion of the long arm of chromosome 2: case report and review of literature.
    Taysi K, Dengler DR, Jones LA, Heersma JR.
    Ann Genet; 1981 Nov 01; 24(4):245-7. PubMed ID: 7036843
    [No Abstract] [Full Text] [Related]

  • 25. Ring chromosome 5 associated with severe growth retardation as the sole major physical abnormality.
    Migliori MV, Cherubini V, Bartolotta E, Pettinari A, Pecora R.
    Am J Med Genet; 1994 Jan 01; 49(1):108-10. PubMed ID: 8172236
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  • 26. [On a case of supernumerary metacentric chromosome. Clinical aspects].
    Cagini P, Fallani M, Vasapollo D.
    Minerva Pediatr; 1974 Aug 18; 26(26):1295-301. PubMed ID: 4212722
    [No Abstract] [Full Text] [Related]

  • 27. Triploidy (69,XXY) in a liveborn infant.
    Simpson JL, Dische R, Morillo-Cucci G, Connolly CE.
    Ann Genet; 1972 Jun 18; 15(2):103-6. PubMed ID: 4557147
    [No Abstract] [Full Text] [Related]

  • 28. Chromosomal aberration involving a member of the D group in a mentally retarded child with multiple congenital anomalies.
    Giorgi PL, Paci A, Ceccarelli M, Vizzoni L.
    Helv Paediatr Acta; 1967 Oct 18; 22(5):466-71. PubMed ID: 5595749
    [No Abstract] [Full Text] [Related]

  • 29. [Supernumerary metacentric small chromosome in a boy with mental retardation].
    Antich J, Sabater J.
    Arch Neurobiol (Madr); 1971 Oct 18; 34(4):315-24. PubMed ID: 4999565
    [No Abstract] [Full Text] [Related]

  • 30. [The clinical picture of 13q22-qter duplication in a 2-year-old boy].
    Halasová E, Lukácová M, Bergendiová E, Kamenická E.
    Cesk Pediatr; 1987 Aug 18; 42(8):477-9. PubMed ID: 3664759
    [No Abstract] [Full Text] [Related]

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  • 32. [Cohen's syndrome: non-causal association with vascular rings].
    Pérez-Caballero Macarrón C, Lozano Giménez C, Quintana Castilla A, Aparicio Meix JM.
    An Esp Pediatr; 2000 Mar 18; 52(3):289-95. PubMed ID: 11003912
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  • 35. De novo paracentric inversion in a microcephalic boy: 46,XY, inv(14)(q13q24).
    Jaeken J, Fryns JP, Standaert L, De Cock P, Van den Berghe H.
    Ann Genet; 1980 Mar 18; 23(2):105-7. PubMed ID: 6967281
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  • 36. Three families with abnormal, inherited chromosomes: 2q+mat, t(Cp+; 13q-)mat and t(3?-;5q+)pat.
    Neu RL, Gardner LI.
    Ann Genet; 1972 Mar 18; 15(1):19-23. PubMed ID: 4402505
    [No Abstract] [Full Text] [Related]

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  • 38. [Equilibrated 2-14 translocation in a mother and partial trisomy of a pair of the short branches of a number 2 chromosome in 2 of her children].
    Stoll C, Messer J, Vors J.
    Ann Genet; 1974 Sep 18; 17(3):193-6. PubMed ID: 4548821
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