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Journal Abstract Search

398 related items for PubMed ID: 15853951

  • 21. Chronic arthritis associated with chromosome deletion 22q11.2 syndrome.
    Pelkonen P, Lahdenne P, Lantto R, Honkanen V.
    J Rheumatol; 2002 Dec; 29(12):2648-50. PubMed ID: 12465167
    [No Abstract] [Full Text] [Related]

  • 22. Memory and learning in children with 22q11.2 deletion syndrome: evidence for ventral and dorsal stream disruption?
    Lajiness-O'Neill RR, Beaulieu I, Titus JB, Asamoah A, Bigler ED, Bawle EV, Pollack R.
    Child Neuropsychol; 2005 Feb; 11(1):55-71. PubMed ID: 15823983
    [Abstract] [Full Text] [Related]

  • 23. The 22q11.2 deletion syndrome: more answers but more questions.
    Fernhoff PM.
    J Pediatr; 2000 Aug; 137(2):145-7. PubMed ID: 10931401
    [No Abstract] [Full Text] [Related]

  • 24. Williams syndrome cognitive profile also characterizes Velocardiofacial/DiGeorge syndrome.
    Bearden CE, Wang PP, Simon TJ.
    Am J Med Genet; 2002 Aug 08; 114(6):689-92. PubMed ID: 12210289
    [No Abstract] [Full Text] [Related]

  • 25. Concurrent microdeletion and duplication of 22q11.2.
    Blennow E, Lagerstedt K, Malmgren H, Sahlén S, Schoumans J, Anderlid B.
    Clin Genet; 2008 Jul 08; 74(1):61-7. PubMed ID: 18445048
    [Abstract] [Full Text] [Related]

  • 26. [Cerebral polymicrogyria and 22q11 deletion syndrome].
    Arriola-Pereda G, Verdú-Pérez A, de Castro-De Castro P.
    Rev Neurol; 2008 Jul 08; 48(4):188-90. PubMed ID: 19226486
    [Abstract] [Full Text] [Related]

  • 27. 22q11.2 microdeletion syndrome is a common cause of renal tract malformations.
    Burtey S.
    Nat Clin Pract Nephrol; 2008 Aug 08; 4(8):E1. PubMed ID: 18654600
    [No Abstract] [Full Text] [Related]

  • 28. [Epilepsy in an adult with chromosome 22q11 micro-deletion].
    Alla P, Philip N, Azulay JP, Attarian S, Pouget J.
    Rev Neurol (Paris); 1999 Nov 08; 155(11):967-70. PubMed ID: 10603642
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  • 30. 22q11 deletion syndrome: is that what they used to call . . . ?
    Umlauf MG.
    Perspect Psychiatr Care; 2008 Oct 08; 44(4):259-66. PubMed ID: 18826464
    [Abstract] [Full Text] [Related]

  • 31. Comparative study of three diagnostic approaches (FISH, STRs and MLPA) in 30 patients with 22q11.2 deletion syndrome.
    Fernández L, Lapunzina P, Arjona D, López Pajares I, García-Guereta L, Elorza D, Burgueros M, De Torres ML, Mori MA, Palomares M, García-Alix A, Delicado A.
    Clin Genet; 2005 Oct 08; 68(4):373-8. PubMed ID: 16143025
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  • 33. Cardiac defects and results of cardiac surgery in 22q11.2 deletion syndrome.
    Carotti A, Digilio MC, Piacentini G, Saffirio C, Di Donato RM, Marino B.
    Dev Disabil Res Rev; 2008 Oct 08; 14(1):35-42. PubMed ID: 18636635
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  • 35. A comparative study of hearing loss in two microdeletion syndromes: velocardiofacial (22q11.2 deletion) and Williams (7q11.23 deletion) syndromes.
    Zarchi O, Attias J, Raveh E, Basel-Vanagaite L, Saporta L, Gothelf D.
    J Pediatr; 2011 Feb 08; 158(2):301-6. PubMed ID: 20846670
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  • 40. Breakpoint Associated with a novel 2.3 Mb deletion in the VCFS region of 22q11 and the role of Alu (SINE) in recurring microdeletions.
    Uddin RK, Zhang Y, Siu VM, Fan YS, O'Reilly RL, Rao J, Singh SM.
    BMC Med Genet; 2006 Mar 02; 7():18. PubMed ID: 16512914
    [Abstract] [Full Text] [Related]

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