BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

417 related articles for article (PubMed ID: 17557238)

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

  • 22. [Cerebral polymicrogyria and 22q11 deletion syndrome].
    Arriola-Pereda G; Verdú-Pérez A; de Castro-De Castro P
    Rev Neurol; 2009 Feb 16-28; 48(4):188-90. PubMed ID: 19226486
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [CATCH22 or 22q11 deletion syndrome. An underdiagnosed and misunderstood disease category with a variable clinical picture].
    Oskarsdóttir S; Fasth A; Belfrage M; Viggedal G; Persson C; Eriksson BO
    Lakartidningen; 1999 Nov; 96(44):4789-93. PubMed ID: 10584540
    [TBL] [Abstract][Full Text] [Related]  

  • 24. 22q11 Deletion in children with cleft lip and palate--is routine screening justified?
    Bashir MA; Hodgkinson PD; Montgomery T; Splitt M
    J Plast Reconstr Aesthet Surg; 2008; 61(2):130-2. PubMed ID: 17707704
    [TBL] [Abstract][Full Text] [Related]  

  • 25. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 26. [Detection and related analysis to chromosome 22q11 microdeletion in patients with congenital heart diseases].
    Xu ZF; Yi L; Mo XM; Hu Y; Wang DJ; Zhu RF; Jiang YZ; Wu X; Wu Z; Shen L; Zhang Y; Zhong XL
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2006 Jun; 23(3):250-5. PubMed ID: 16767657
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Deletion 22q11: spectrum of associated disorders.
    Hay BN
    Semin Pediatr Neurol; 2007 Sep; 14(3):136-9. PubMed ID: 17980310
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Abdominal lymphatic dysplasia and 22q11 microdeletion.
    Mansir T; Lacombe D; Lamireau T; Taine L; Chateil JF; Le Bail B; Demarquez JL; Fayon M
    Genet Couns; 1999; 10(1):67-70. PubMed ID: 10191431
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Use of amniocytes for prenatal diagnosis of 22q11.2 microdeletion syndrome: a feasibility study.
    Liu T; Liu Q; Wang YX; Yang D; Xin Y; Fang Z; Ding SF; Yang JF
    Chin Med J (Engl); 2010 Feb; 123(4):438-42. PubMed ID: 20193483
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [Neonatal hypocalcaemic dilated myocardiopathy due to a 22q11 microdeletion].
    Goulet M; Rio M; Jacquette A; Ladouceur M; Bonnet D
    Arch Mal Coeur Vaiss; 2006 May; 99(5):520-2. PubMed ID: 16802747
    [TBL] [Abstract][Full Text] [Related]  

  • 31. [Congenital cardiovascular malformations and chromosome microdeletions in 22q11.2].
    Trost D; Engels H; Bauriedel G; Wiebe W; Schwanitz G
    Dtsch Med Wochenschr; 1999 Jan; 124(1-2):3-7. PubMed ID: 9951451
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Fragile X syndrome and 22q11.2 microdeletion in the same sibship.
    Missirian C; Moncla A; Voelckel MA; Ravix V; Philip N
    Am J Med Genet; 2000 Dec; 95(4):358-60. PubMed ID: 11186890
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Incidence and significance of 22q11.2 hemizygosity in patients with interrupted aortic arch.
    Rauch A; Hofbeck M; Leipold G; Klinge J; Trautmann U; Kirsch M; Singer H; Pfeiffer RA
    Am J Med Genet; 1998 Jul; 78(4):322-31. PubMed ID: 9714433
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [Prenatal diagnosis of 22q11 microdeletion syndrome].
    Cai M; Huang H; Lin N; Guo N; Wu X; Su L; Xu L
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Apr; 34(2):192-195. PubMed ID: 28397216
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [Epilepsy in an adult with chromosome 22q11 micro-deletion].
    Alla P; Philip N; Azulay JP; Attarian S; Pouget J
    Rev Neurol (Paris); 1999 Nov; 155(11):967-70. PubMed ID: 10603642
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Microdeletion and microduplication 22q11.2 screening in 295 patients with clinical features of DiGeorge/Velocardiofacial syndrome.
    Brunet A; Gabau E; Perich RM; Valdesoiro L; Brun C; Caballín MR; Guitart M
    Am J Med Genet A; 2006 Nov; 140(22):2426-32. PubMed ID: 17041934
    [TBL] [Abstract][Full Text] [Related]  

  • 38. The 22q11.2 Deletion Syndrome in Congenital Heart Defects: Prevalence of Microdeletion Syndrome in Cameroon.
    Wonkam A; Toko R; Chelo D; Tekendo-Ngongang C; Kingue S; Dahoun S
    Glob Heart; 2017 Jun; 12(2):115-120. PubMed ID: 28302550
    [TBL] [Abstract][Full Text] [Related]  

  • 39. FISH investigation of 22q11.2 deletion in patients with immunodeficiency and/or cardiac abnormalities.
    Yakut T; Kilic SS; Cil E; Yapici E; Egeli U
    Pediatr Surg Int; 2006 Apr; 22(4):380-3. PubMed ID: 16463032
    [TBL] [Abstract][Full Text] [Related]  

  • 40. The 22q11.2 deletion syndrome.
    Emanuel BS; McDonald-McGinn D; Saitta SC; Zackai EH
    Adv Pediatr; 2001; 48():39-73. PubMed ID: 11480765
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 21.