BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

626 related articles for article (PubMed ID: 15523900)

  • 1. Detection of 22q11.2 deletion among 139 patients with Di George/Velocardiofacial syndrome features.
    Kitsiou-Tzeli S; Kolialexi A; Fryssira H; Galla-Voumvouraki A; Salavoura K; Kanariou M; Tsangaris GT; Kanavakis E; Mavrou A
    In Vivo; 2004; 18(5):603-8. PubMed ID: 15523900
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Chromosome 22q11.2 microdeletions in velocardiofacial syndrome patients with widely variable manifestations.
    Ravnan JB; Chen E; Golabi M; Lebo RV
    Am J Med Genet; 1996 Dec; 66(3):250-6. PubMed ID: 8985481
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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; 42(3):215-8. PubMed ID: 11105620
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Dual-probe fluorescence in situ hybridization assay for detecting deletions associated with VCFS/DiGeorge syndrome I and DiGeorge syndrome II loci.
    Berend SA; Spikes AS; Kashork CD; Wu JM; Daw SC; Scambler PJ; Shaffer LG
    Am J Med Genet; 2000 Apr; 91(4):313-7. PubMed ID: 10766989
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Clinical heterogeneity of the chromosome 22q11 microdeletion syndrome].
    Muñoz S; Garay F; Flores I; Heusser F; Talesnik E; Aracena M; Mellado C; Méndez C; Arnaiz P; Repetto G
    Rev Med Chil; 2001 May; 129(5):515-21. PubMed ID: 11464533
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. [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]  

  • 11. [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]  

  • 12. Microdeletion 22q11 and oesophageal atresia.
    Digilio MC; Marino B; Bagolan P; Giannotti A; Dallapiccola B
    J Med Genet; 1999 Feb; 36(2):137-9. PubMed ID: 10051013
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Di George anomaly and velocardiofacial syndrome.
    Stevens CA; Carey JC; Shigeoka AO
    Pediatrics; 1990 Apr; 85(4):526-30. PubMed ID: 2314965
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Study on clinical features and fluorescence in situ hybridization detections of 22q11 microdeletion syndrome].
    Qin YF; Yang JB; Xie CH; Shao J; Zhao ZY
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Jun; 24(3):284-7. PubMed ID: 17557238
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. DiGeorge syndrome: new insights.
    Goldmuntz E
    Clin Perinatol; 2005 Dec; 32(4):963-78, ix-x. PubMed ID: 16325672
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Velo-cardio-facial syndrome and DiGeorge sequence with meningomyelocele and deletions of the 22q11 region.
    Nickel RE; Pillers DA; Merkens M; Magenis RE; Driscoll DA; Emanuel BS; Zonana J
    Am J Med Genet; 1994 Oct; 52(4):445-9. PubMed ID: 7747757
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Chromosome 22q11 deletions in patients with selected outflow tract malformations.
    Frohn-Mulder IM; Wesby Swaay E; Bouwhuis C; Van Hemel JO; Gerritsma E; Niermeyer MF; Hess J
    Genet Couns; 1999; 10(1):35-41. PubMed ID: 10191427
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [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 Oct 1-15; 37(7):601-7. PubMed ID: 14582013
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [22q11.2 chromosome deletion and velo-cardio-facial syndrome in a patient with tetralogy of Fallot].
    Morava E; Masszi G; Czakó M; Tóth G; Melegh B; Kosztolányi G
    Orv Hetil; 2000 Aug; 141(34):1873-5. PubMed ID: 11006712
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 32.