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Journal Abstract Search

137 related items for PubMed ID: 10885509

  • 1. Pericentric inversion in human chromosome 8 and spherocytosis.
    Ganguly BB, Dalvi R, Mehta AV.
    Cytobios; 2000; 102(400):119-26. PubMed ID: 10885509
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  • 4. A child with recombinant of chromosome 8 inherited from a carrier mother with a pericentric inversion.
    Lovell M, Herrera J, Coco R.
    Medicina (B Aires); 1982; 42(4):359-62. PubMed ID: 15171014
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  • 5. [Cytogenetic study of a case of Fanconi's syndrome with a familial pericentric inversion].
    Crippa L, Ferrier S.
    J Genet Hum; 1975 Mar; 23(1):7-16. PubMed ID: 1165481
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  • 7. [Pericentric inversion of chromosome 9. Summary of the authors' results].
    Vargas de los Monteros MT, Fernández-Novoa García MC, Salas Herrero E, San Martín Díez MV, Novales Huertas MA.
    An Esp Pediatr; 1990 Nov; 33(5):442-9. PubMed ID: 2096758
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  • 8. High recurrence of recombinants in a family with pericentric inversion of chromosome 18.
    Mejía-Baltodano G, Bobadilla L, Gonzalez RM, Barros-Núñez P.
    Ann Genet; 1997 Nov; 40(3):164-8. PubMed ID: 9401106
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  • 13. [Double trisomy and transmitted pericentric inversion (48,XXY, +21,inv(22)). Interchromosomal effect].
    Saura R, Longy M, Sautarael M, Renouil M, Sandler B.
    Ann Genet; 1983 Nov; 26(3):180-2. PubMed ID: 6606381
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  • 14. Meiotic segregation analysis in spermatozoa of pericentric inversion carriers using fluorescence in-situ hybridization.
    Morel F, Laudier B, Guérif F, Couet ML, Royère D, Roux C, Bresson JL, Amice V, De Braekeleer M, Douet-Guilbert N.
    Hum Reprod; 2007 Jan; 22(1):136-41. PubMed ID: 16917123
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  • 17. Prenatal detection of de novo inversion of chromosome (2) (p13q11.2) and postnatal follow-up.
    Kozma C, Subasinghe C, Meck J.
    Prenat Diagn; 1996 Apr; 16(4):366-70. PubMed ID: 8734815
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  • 19. Unbalanced inherited complex chromosome rearrangement involving chromosome 8, 10, 11 and 16 in a patient with congenital malformations and delayed development.
    Karmous-Benailly H, Giuliano F, Massol C, Bloch C, De Ricaud D, Lambert JC, Perelman S.
    Eur J Med Genet; 2006 Apr; 49(5):431-8. PubMed ID: 16497571
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  • 20. Two unbalanced segregation products due to a maternal t(7;16)inv(16).
    Leegte B, Sikkema-Raddatz B, Hordijk R, Davelaar I, van der Veen A, Cobben JM.
    Prenat Diagn; 2001 Jul; 21(7):550-2. PubMed ID: 11494289
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