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Journal Abstract Search

132 related items for PubMed ID: 11856871

  • 1. Molecular and cytogenetic characterisation of a small interstitial de novo 20p13-->p12.3 deletion in a patient with severe growth deficit.
    Leprêtre F, Montpellier C, Delannoy V, Froguel P, Vasseur F.
    Cytogenet Cell Genet; 2001; 94(3-4):142-6. PubMed ID: 11856871
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  • 4. Molecular cytogenetic analysis of a de novo interstitial chromosome 10q22 deletion.
    Tzschach A, Krause-Plonka I, Menzel C, Knoblauch A, Toennies H, Hoeltzenbein M, Radke M, Ropers HH, Kalscheuer V.
    Am J Med Genet A; 2006 May 15; 140(10):1108-10. PubMed ID: 16619204
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  • 5. Molecular and cytogenetic analysis of an interstitial 20p deletion associated with syndromic intrahepatic ductular hypoplasia (Alagille syndrome).
    Schnittger S, Höfers C, Heidemann P, Beermann F, Hansmann I.
    Hum Genet; 1989 Oct 15; 83(3):239-44. PubMed ID: 2793167
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  • 6. Autistic disorder and chromosomal mosaicism 46,XY[123]/46,XY,del(20)(pter --> p12.2)[10].
    Sauter S, von Beust G, Burfeind P, Weise A, Starke H, Liehr T, Zoll B.
    Am J Med Genet A; 2003 Aug 01; 120A(4):533-6. PubMed ID: 12884434
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  • 7. Molecular cytogenetic characterization of the first reported case of inv dup del 20p compatible with a U-type exchange model.
    Leclercq S, Maincent K, Baverel F, Tessier DL, Letourneur F, Lebbar A, Dupont JM.
    Am J Med Genet A; 2009 Mar 01; 149A(3):437-45. PubMed ID: 19206177
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  • 8. Molecular cytogenetic analysis of a constitutional de novo interstitial deletion of chromosome 12p in a boy with developmental delay and congenital anomalies.
    Gläser B, Rossier E, Barbi G, Chiaie LD, Blank C, Vogel W, Kehrer-Sawatzki H.
    Am J Med Genet A; 2003 Jan 01; 116A(1):66-70. PubMed ID: 12476454
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  • 9. A de novo interstitial deletion of chromosome 15 band q25 as revealed by FISH-technique.
    Verma RS, Kleyman SM, Giridharan R, Ramesh KH.
    Clin Genet; 1996 Jun 01; 49(6):303-5. PubMed ID: 8884079
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  • 13. Alagille syndrome with deletion 20p12.2-p12.3 and hypoplastic left heart.
    Robert ML, Lopez T, Crolla J, Huang S, Owen C, Burvill-Holmes L, Stumper O, Turnpenny PD.
    Clin Dysmorphol; 2007 Oct 01; 16(4):241-6. PubMed ID: 17786115
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  • 14. Deletions of 20p12 in Alagille syndrome: frequency and molecular characterization.
    Krantz ID, Rand EB, Genin A, Hunt P, Jones M, Louis AA, Graham JM, Bhatt S, Piccoli DA, Spinner NB.
    Am J Med Genet; 1997 May 02; 70(1):80-6. PubMed ID: 9129746
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  • 16. An interstitial deletion of chromosome 7 at band q21: a case report and review.
    Courtens W, Vermeulen S, Wuyts W, Messiaen L, Wauters J, Nuytinck L, Peeters N, Storm K, Speleman F, Nöthen MM.
    Am J Med Genet A; 2005 Apr 01; 134A(1):12-23. PubMed ID: 15732063
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  • 18. Identification of cryptic rearrangements in patients with 18q- deletion syndrome.
    Brkanac Z, Cody JD, Leach RJ, DuPont BR.
    Am J Hum Genet; 1998 Jun 01; 62(6):1500-6. PubMed ID: 9585582
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  • 19. 20p12.3 deletion is rare cause of syndromic cleft palate: case report and review of literature.
    Amasdl S, Natiq A, Sbiti A, Zerkaoui M, Lyahyai J, Amzazi S, Liehr T, Sefiani A.
    BMC Res Notes; 2016 Jan 02; 9():5. PubMed ID: 26724919
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  • 20. Perinatal findings and molecular cytogenetic analyses of de novo interstitial deletion of 9q (9q22.3-->q31.3) associated with Gorlin syndrome.
    Chen CP, Lin SP, Wang TH, Chen YJ, Chen M, Wang W.
    Prenat Diagn; 2006 Aug 02; 26(8):725-9. PubMed ID: 16927391
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