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Journal Abstract Search

194 related items for PubMed ID: 6345474

  • 1. Partial monosomy for a 21 chromosome. Report of a new case of r(21) and review of the literature.
    Ferrante E, Vignetti P, Antonelli M, Bruni L, Bertasi S, Chessa L.
    Helv Paediatr Acta; 1983 Mar; 38(1):73-80. PubMed ID: 6345474
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  • 2. [Ring chromosome 13 and multiple malformations (author's transl)].
    Antich J, Plaza J, Geán E.
    An Esp Pediatr; 1981 Nov; 15(5):469-73. PubMed ID: 7332149
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  • 5. ["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; 12(5):463-8. PubMed ID: 464416
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  • 6. De novo partial monosomy 21 with unusual karyotype.
    Al-Awadi SA, Naguib KK, Teebi AS, Sundareshan TS.
    Jinrui Idengaku Zasshi; 1986 Mar; 31(1):45-8. PubMed ID: 3735757
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  • 11. [Clinical picture of partial monosomy of chromosome 11 q].
    Dörr U.
    Monatsschr Kinderheilkd; 1986 Nov; 134(11):808-11. PubMed ID: 3807920
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  • 12. A case of acute myeloblastic leukemia with chromosomes showing 46, XY = 11/46, XY, 21q- = 39.
    Tadano J, Niwa M, Nagumo F, Watanabe K, Arimori S.
    Tokai J Exp Clin Med; 1980 Jan; 5(1):45-50. PubMed ID: 6930118
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  • 13. Partial monosomy of a G group chromosome (45,XY,G-46,XY,Gr): report of a new case.
    Armendares S, Buentello L, Cantu-Garza JM.
    Ann Genet; 1971 Mar; 14(1):7-12. PubMed ID: 5314299
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  • 14. Clinical findings and cytogenetic analysis of small supernumerary ring chromosomes 7: report of two new cases.
    Chantot-Bastaraud S, Muti C, Pipiras E, Routon MC, Roubergue A, Burglen L, Siffroi JP, Simon-Bouy B.
    Ann Genet; 2004 Mar; 47(3):241-9. PubMed ID: 15337469
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  • 15. Clinical features of monosomy 10qter.
    Zatterale A, Pagano L, Fioretti G, Caniglia M, Festa B, Renda S, Rinaldi MM, Ventruto V.
    Ann Genet; 1983 Mar; 26(2):106-8. PubMed ID: 6604483
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  • 16. Elucidation of the cytogenetic abnormality in a 4p- "phenocopy".
    Curry CJ, Ying KL, O'Lague P, Tsai J.
    Birth Defects Orig Artic Ser; 1982 Mar; 18(3B):275-86. PubMed ID: 7139110
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  • 19. De novo tandem duplication of the middle segment of the long arm of chromosome 14.
    Ito M, Mutoh K, Okuno T, Mikawa H, Edagawa J, Abe T.
    Ann Genet; 1983 Mar; 26(2):116-9. PubMed ID: 6604486
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  • 20. [Ring chromosome 8: microcephaly, mental retardation and minor facial anomalies with adhesive behavioral phenotype].
    Bibas Bonet H, Fontenla M, Fauze R, G de Pinat I.
    Rev Neurol; 1983 Mar; 32(8):746-50. PubMed ID: 11391511
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