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Journal Abstract Search

137 related items for PubMed ID: 6967281

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  • 3. Prenatal detection of de novo paracentric inversion 46, XX inv (14) (q22q32.1) in a normal child: report and review of the literature.
    Hales HA, Peterson CM, Carey J, Hecht BK, Hecht F.
    Am J Med Genet; 1993 Nov 01; 47(6):848-51. PubMed ID: 8279482
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  • 4. U-type exchange in a paracentric inversion as a possible mechanism of origin of an inverted tandem duplication of chromosome 8.
    Mitchell JJ, Vekemans M, Luscombe S, Hayden M, Weber B, Richter A, Sparkes R, Kojis T, Watters G, Der Kaloustian VM.
    Am J Med Genet; 1994 Feb 15; 49(4):384-7. PubMed ID: 8160729
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  • 5. A familial paracentric inv(1)(q42q44) resulting in a child with a del(1)(q42) karyotype.
    Speevak M, Hunter AG, Hughes H, Cox DM.
    Ann Genet; 1985 Feb 15; 28(3):177-80. PubMed ID: 3879153
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  • 8. Unexpected identification of two interstitial deletions in a patient with a pericentric inversion of a chromosome 4 and an abnormal phenotype.
    Piovani G, Borsani G, Bertini V, Kalscheuer VM, Viertel P, Bellotti D, Valseriati D, Barlati S.
    Eur J Med Genet; 2006 Feb 15; 49(3):215-23. PubMed ID: 16762823
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  • 9. Three unrelated cases of paracentric inversions of 1p in individuals with abnormal phenotypes.
    Estop AM, Bansal V, Lin A, Levinson F, Karlin SM, Surti U, Wenger SL, Steele MW.
    Am J Med Genet; 1994 Feb 15; 49(4):410-3. PubMed ID: 8160735
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  • 10. De novo pericentric inversion of chromosome 4, inv(4)(p16q12) in a boy with piebaldism and mental retardation.
    Ramadevi AR, Naik U, Dutta U, Srikanth, Prabhakara K.
    Am J Med Genet; 2002 Nov 22; 113(2):190-2. PubMed ID: 12407711
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  • 12. [A single D chromosome in ring form in a 2-year-old girl with mental retardation].
    Morić-Petrović S, Garzicić B, Despotović M, Kalicanin P.
    Srp Arh Celok Lek; 1970 Mar 22; 98(3):447-52. PubMed ID: 5205520
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  • 13. Recombinant chromosome 9 possibly derived from breakage and reunion of sister chromatids within a paracentric inversion loop.
    Phelan MC, Stevenson RE, Anderson EV.
    Am J Med Genet; 1993 May 15; 46(3):304-8. PubMed ID: 8488876
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  • 14. Duplication of (2)(q11.1-q13.2) in a boy with mental retardation and cleft lip and palate: another clefting gene locus on proximal 2q?
    Riegel M, Schinzel A.
    Am J Med Genet; 2002 Jul 22; 111(1):76-80. PubMed ID: 12124740
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  • 15. Familial paracentric inversion of the short arm of chromosome 3.
    Fryns JP, van den Berghe H.
    Ann Genet; 1979 Jul 22; 22(3):163-4. PubMed ID: 316673
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  • 16. De novo satellited 21q associated with corpus callosum dysgenesis, colpocephaly, a concealed penis, congenital heart defects, and developmental delay.
    Chen CP, Lin SP, Chern SR, Lee CC, Huang JK, Wang W, Liao YW.
    Genet Couns; 2004 Jul 22; 15(4):437-42. PubMed ID: 15658619
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  • 20. Concurrence of inv(7)(q11.2q32) and del(8)(p23.1) in a girl with congenital microcephaly, hypotonia, developmental delay, strabismus, hypernatremia, hypermagnesemia and deafness.
    Mahjoubi F, Nasiri F, Razazian F.
    Genet Couns; 2012 Jul 22; 23(3):397-404. PubMed ID: 23072189
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