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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

104 related items for PubMed ID: 8773902

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  • 28. No justification of routine screening for 22q11 deletions in patients with overt cleft palate.
    Ruiter EM, Bongers EM, Smeets D, Kuijpers-Jagtman AM, Hamel BC.
    Clin Genet; 2003 Sep; 64(3):216-9. PubMed ID: 12919136
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  • 29. [Phenotypic variability of deletion 22q11.2. An analysis of 16 observations with special emphasis on the neurological manifestations].
    Eirís-Puñal J, Iglesias-Meleiro JM, Blanco-Barca MO, Fuster-Siebert M, Barros-Angueira F, Ansede A, Castro-Gago M.
    Rev Neurol; 2003 Sep; 37(7):601-7. PubMed ID: 14582013
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  • 32. Palate abnormalities in Chilean patients with chromosome 22q11 microdeletion syndrome.
    Lay-Son G, Palomares M, Guzman ML, Vasquez M, Puga A, Repetto GM.
    Int J Pediatr Otorhinolaryngol; 2012 Dec; 76(12):1726-8. PubMed ID: 22939891
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  • 35. Catch 22--microdeletion 22q11 screening in patients with congenital heart defects.
    Von Beust G, Bartmus D, Bartels I.
    Genet Couns; 1998 Dec; 9(3):223-7. PubMed ID: 9777346
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  • 37. CATCHing a break on 22.
    Glover TW.
    Nat Genet; 1995 Jul; 10(3):257-8. PubMed ID: 7670460
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  • 38. Neural tube defects and deletions of 22q11.
    Nickel RE, Magenis RE.
    Am J Med Genet; 1996 Dec 02; 66(1):25-7. PubMed ID: 8957506
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  • 39. Microsatellite DNA markers detects 95% of chromosome 22q11 deletions.
    Bonnet D, Cormier-Daire V, Kachaner J, Szezepanski I, Souillard P, Sidi D, Munnich A, Lyonnet S.
    Am J Med Genet; 1997 Jan 20; 68(2):182-4. PubMed ID: 9028455
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  • 40. Congenital heart defects and chromosomal anomalies including 22q11 microdeletion (CATCH 22).
    Soares G, Alvares S, Rocha C, Teixeira MF, Mota MC, Reis MI, Feijó MJ, Lima MR, Pinto MR.
    Rev Port Cardiol; 2005 Mar 20; 24(3):349-71. PubMed ID: 15929620
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