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Journal Abstract Search

194 related items for PubMed ID: 19486360

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  • 2. Microdeletion of chromosome 15q26.1 in a child with intractable generalized epilepsy.
    Dhamija R, Breningstall G, Wong-Kisiel L, Dolan M, Hirsch B, Wirrell E.
    Pediatr Neurol; 2011 Jul; 45(1):60-2. PubMed ID: 21723464
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  • 8. 6q terminal deletion syndrome associated with a distinctive EEG and clinical pattern: a report of five cases.
    Elia M, Striano P, Fichera M, Gaggero R, Castiglia L, Galesi O, Malacarne M, Pierluigi M, Amato C, Musumeci SA, Romano C, Majore S, Grammatico P, Zara F, Striano S, Faravelli F.
    Epilepsia; 2006 May; 47(5):830-8. PubMed ID: 16686647
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  • 9. Distal 4p microdeletion in a case of Wolf-Hirschhorn syndrome with congenital diaphragmatic hernia.
    Casaccia G, Mobili L, Braguglia A, Santoro F, Bagolan P.
    Birth Defects Res A Clin Mol Teratol; 2006 Mar; 76(3):210-3. PubMed ID: 16498629
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  • 11. Narrowing the deleted region associated with the 15q21 syndrome.
    Pramparo T, Mattina T, Gimelli S, Liehr T, Zuffardi O.
    Eur J Med Genet; 2005 Mar; 48(3):346-52. PubMed ID: 16179230
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  • 12. Further delineation of deletion 1p36 syndrome in 60 patients: a recognizable phenotype and common cause of developmental delay and mental retardation.
    Battaglia A, Hoyme HE, Dallapiccola B, Zackai E, Hudgins L, McDonald-McGinn D, Bahi-Buisson N, Romano C, Williams CA, Brailey LL, Zuberi SM, Carey JC.
    Pediatrics; 2008 Feb; 121(2):404-10. PubMed ID: 18245432
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  • 13. Construction of a natural panel of 11p11.2 deletions and further delineation of the critical region involved in Potocki-Shaffer syndrome.
    Wakui K, Gregato G, Ballif BC, Glotzbach CD, Bailey KA, Kuo PL, Sue WC, Sheffield LJ, Irons M, Gomez EG, Hecht JT, Potocki L, Shaffer LG.
    Eur J Hum Genet; 2005 May; 13(5):528-40. PubMed ID: 15852040
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  • 14. Fryns syndrome phenotype caused by chromosome microdeletions at 15q26.2 and 8p23.1.
    Slavotinek A, Lee SS, Davis R, Shrit A, Leppig KA, Rhim J, Jasnosz K, Albertson D, Pinkel D.
    J Med Genet; 2005 Sep; 42(9):730-6. PubMed ID: 16141010
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  • 16. New cases and refinement of the critical region in the 1q41q42 microdeletion syndrome.
    Rosenfeld JA, Lacassie Y, El-Khechen D, Escobar LF, Reggin J, Heuer C, Chen E, Jenkins LS, Collins AT, Zinner S, Babcock M, Morrow B, Schultz RA, Torchia BS, Ballif BC, Tsuchiya KD, Shaffer LG.
    Eur J Med Genet; 2011 Sep; 54(1):42-9. PubMed ID: 20951845
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  • 17. An emerging 1q21.1 deletion-associated neurodevelopmental phenotype.
    Basel-Vanagaite L, Goldberg-Stern H, Mimouni-Bloch A, Shkalim V, Böhm D, Kohlhase J.
    J Child Neurol; 2011 Jan; 26(1):113-6. PubMed ID: 21212457
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  • 18. Array-CGH analysis and clinical description of 2q37.3 de novo subtelomeric deletion.
    Kitsiou-Tzeli S, Sismani C, Ioannides M, Bashiardes S, Ketoni A, Touliatou V, Kolialexi A, Mavrou A, Kanavakis E, Patsalis PC.
    Eur J Med Genet; 2007 Jan; 50(1):73-8. PubMed ID: 17194633
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  • 20. Interstitial deletion of 18q: comparative genomic hybridization array analysis of 46, XX,del(18)(q21.2.q21.33).
    Kato Z, Morimoto W, Kimura T, Matsushima A, Kondo N.
    Birth Defects Res A Clin Mol Teratol; 2010 Feb; 88(2):132-5. PubMed ID: 19813260
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