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Journal Abstract Search

747 related items for PubMed ID: 10191425

  • 1. The Philadelphia story: the 22q11.2 deletion: report on 250 patients.
    McDonald-McGinn DM, Kirschner R, Goldmuntz E, Sullivan K, Eicher P, Gerdes M, Moss E, Solot C, Wang P, Jacobs I, Handler S, Knightly C, Heher K, Wilson M, Ming JE, Grace K, Driscoll D, Pasquariello P, Randall P, Larossa D, Emanuel BS, Zackai EH.
    Genet Couns; 1999; 10(1):11-24. PubMed ID: 10191425
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  • 2. The deletions of 22q11--the Portuguese experience.
    Gaspar IM, Lourenço MT, Reis MI, Soares MA, Nogueira G, Ferreira F, Feijóo MJ.
    Genet Couns; 1999; 10(1):51-7. PubMed ID: 10191429
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  • 3. The 22q11.2 deletion: screening, diagnostic workup, and outcome of results; report on 181 patients.
    McDonald-McGinn DM, LaRossa D, Goldmuntz E, Sullivan K, Eicher P, Gerdes M, Moss E, Wang P, Solot C, Schultz P, Lynch D, Bingham P, Keenan G, Weinzimer S, Ming JE, Driscoll D, Clark BJ, Markowitz R, Cohen A, Moshang T, Pasquariello P, Randall P, Emanuel BS, Zackai EH.
    Genet Test; 1997; 1(2):99-108. PubMed ID: 10464633
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  • 4. Congenital heart defects in patients with DiGeorge/velocardiofacial syndrome and del22q11.
    Marino B, Digilio MC, Toscano A, Giannotti A, Dallapiccola B.
    Genet Couns; 1999; 10(1):25-33. PubMed ID: 10191426
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  • 5. Retrospective analysis of feeding and speech disorders in 50 patients with velo-cardio-facial syndrome.
    Rommel N, Vantrappen G, Swillen A, Devriendt K, Feenstra L, Fryns JP.
    Genet Couns; 1999; 10(1):71-8. PubMed ID: 10191432
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  • 8. 22q11 deletion in DGS/VCFS monozygotic twins with discordant phenotypes.
    Vincent MC, Heitz F, Tricoire J, Bourrouillou G, Kuhlein E, Rolland M, Calvas P.
    Genet Couns; 1999; 10(1):43-9. PubMed ID: 10191428
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  • 10. CATCH 22: deletion of locus 22q11 in velocardiofacial syndrome, DiGeorge anomaly, and nonsyndromic conotruncal defects.
    Hou JW, Wang JK, Tsai WY, Chou CC, Wang TR.
    J Formos Med Assoc; 1997 Jun; 96(6):419-23. PubMed ID: 9216164
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  • 11. Clinical correlation of chromosome 22q11.2 fluorescent in situ hybridization analysis and velocardiofacial syndrome.
    Oh AK, Workman LA, Wong GB.
    Cleft Palate Craniofac J; 2007 Jan; 44(1):62-6. PubMed ID: 17214538
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  • 12. CATCH 22 syndrome: report of 7 infants with follow-up data and review of the recent advancements in the genetic knowledge of the locus 22q11.
    Sergi C, Serpi M, Müller-Navia J, Schnabel PA, Hagl S, Otto HF, Ulmer HE.
    Pathologica; 1999 Jun; 91(3):166-72. PubMed ID: 10536461
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  • 13. [Microdeletion of 22q11, DiGeorge and velocardiofacial syndrome].
    Hjalgrim H, Hahnemann JM, Timshel S, Brøndum-Nielsen K.
    Ugeskr Laeger; 2000 Jul 31; 162(31):4169-70. PubMed ID: 10962926
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  • 14. Microdeletion of 22q11 (CATCH 22) in children with conotruncal heart defect and extracardiac malformations.
    Alikaşifoğlu M, Malkoç N, Ceviz N, Ozme S, Uludoğan S, Tunçbilek E.
    Turk J Pediatr; 2000 Jul 31; 42(3):215-8. PubMed ID: 11105620
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  • 17. Presenting symptoms and clinical features in 130 patients with the velo-cardio-facial syndrome. The Leuven experience.
    Vantrappen G, Devriendt K, Swillen A, Rommel N, Vogels A, Eyskens B, Gewillig M, Feenstra L, Fryns JP.
    Genet Couns; 1999 Jul 31; 10(1):3-9. PubMed ID: 10191424
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  • 20. DiGeorge syndrome: new insights.
    Goldmuntz E.
    Clin Perinatol; 2005 Dec 31; 32(4):963-78, ix-x. PubMed ID: 16325672
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