BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

492 related articles for article (PubMed ID: 25715476)

  • 21. Copy number variations and risk for schizophrenia in 22q11.2 deletion syndrome.
    Bassett AS; Marshall CR; Lionel AC; Chow EW; Scherer SW
    Hum Mol Genet; 2008 Dec; 17(24):4045-53. PubMed ID: 18806272
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Detecting 22q11.2 Deletion Syndrome in Newborns with Low T Cell Receptor Excision Circles from Severe Combined Immunodeficiency Screening.
    Liao HC; Liao CH; Kao SM; Chiang CC; Chen YJ
    J Pediatr; 2019 Jan; 204():219-224.e1. PubMed ID: 30268402
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Pre- and Postnatal Diagnosis of 10p14 Deletion and 22q11.2 Deletion Syndrome and Significance of Non-Cardiac Markers.
    Shetty M; Srikanth A; Kadandale J; Hegde S
    Cytogenet Genome Res; 2016; 148(4):249-55. PubMed ID: 27300488
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Screening of 22q11.2DS Using Multiplex Ligation-Dependent Probe Amplification as an Alternative Diagnostic Method.
    Maran S; Faten SA; Lim SE; Lai KS; Ibrahim WPW; Ankathil R; Gan SH; Tan HL
    Biomed Res Int; 2020; 2020():6945730. PubMed ID: 33062692
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Inherited t(9;22) as the cause of DiGeorge syndrome: a case report.
    Shuib S; Abdul Latif Z; Abidin NZ; Akmal SN; Zakaria Z
    Malays J Pathol; 2009 Dec; 31(2):133-6. PubMed ID: 20514857
    [TBL] [Abstract][Full Text] [Related]  

  • 26. [Improvement of genetic diagnostic strategy in velo-cardio-facial syndrome].
    Pânzaru M; Rusu C; Voloşciuc M; Braha E; Butnariu L; Ivanov I; Grămescu M; Popescu R; Caba L; Sireteanu A; Macovei M; Covic M; Gorduza EV
    Rev Med Chir Soc Med Nat Iasi; 2011; 115(3):756-61. PubMed ID: 22046783
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Improving the Diagnosis of Children with 22q11.2 Deletion Syndrome: A Single-center Experience from Serbia.
    Cuturilo G; Drakulic D; Jovanovic I; Krstic A; Djukic M; Skoric D; Mijovic M; Stefanovic I; Milivojevic M; Stevanovic M
    Indian Pediatr; 2016 Sep; 53(9):786-789. PubMed ID: 27771646
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 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]  

  • 29. 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]  

  • 30. Detecting 22q11.2 deletion in Chinese children with conotruncal heart defects and single nucleotide polymorphisms in the haploid TBX1 locus.
    Xu YJ; Wang J; Xu R; Zhao PJ; Wang XK; Sun HJ; Bao LM; Shen J; Fu QH; Li F; Sun K
    BMC Med Genet; 2011 Dec; 12():169. PubMed ID: 22185286
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Left pulmonary artery in 22q11.2 deletion syndrome. Echocardiographic evaluation in patients without cardiac defects and role of Tbx1 in mice.
    Mastromoro G; Calcagni G; Versacci P; Putotto C; Chinali M; Lambiase C; Unolt M; Pelliccione E; Anaclerio S; Caprio C; Cioffi S; Bilio M; Baban A; Drago F; Digilio MC; Marino B; Baldini A
    PLoS One; 2019; 14(4):e0211170. PubMed ID: 30933971
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Defining new guidelines for screening the 22q11.2 deletion based on a clinical and dysmorphologic evaluation of 194 individuals and review of the literature.
    Monteiro FP; Vieira TP; Sgardioli IC; Molck MC; Damiano AP; Souza J; Monlleó IL; Fontes MI; Fett-Conte AC; Félix TM; Leal GF; Ribeiro EM; Banzato CE; Dantas Cde R; Lopes-Cendes I; Gil-da-Silva-Lopes VL
    Eur J Pediatr; 2013 Jul; 172(7):927-45. PubMed ID: 23440478
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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]  

  • 34. 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; 68(2):182-4. PubMed ID: 9028455
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Submicroscopic deletions at 22q11.2: variability of the clinical picture and delineation of a commonly deleted region.
    Lindsay EA; Greenberg F; Shaffer LG; Shapira SK; Scambler PJ; Baldini A
    Am J Med Genet; 1995 Mar; 56(2):191-7. PubMed ID: 7625444
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Use of fluorescence in situ hybridization (FISH) in the diagnosis of DiGeorge sequence and related diseases.
    Larson RS; Butler MG
    Diagn Mol Pathol; 1995 Dec; 4(4):274-8. PubMed ID: 8634784
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Human TBX1 missense mutations cause gain of function resulting in the same phenotype as 22q11.2 deletions.
    Zweier C; Sticht H; Aydin-Yaylagül I; Campbell CE; Rauch A
    Am J Hum Genet; 2007 Mar; 80(3):510-7. PubMed ID: 17273972
    [TBL] [Abstract][Full Text] [Related]  

  • 38. 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]  

  • 39. Central 22q11.2 deletion (LCR22 B-D) in a fetus with severe fetal growth restriction and a mother with severe systemic lupus erythematosus: Further evidence of CRKL haploinsufficiency in the pathogenesis of 22q11.2 deletion syndrome.
    Lin I; Afshar Y; Goldstein J; Grossman J; Grody WW; Quintero-Rivera F
    Am J Med Genet A; 2021 Oct; 185(10):3042-3047. PubMed ID: 34196458
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Atypical presentations of 22q11.2 deletion syndrome: explaining the genetic defects and genome architecture.
    Tuţulan-Cuniţă AC; Budişteanu M; Papuc SM; Dupont JM; Blancho D; Lebbar A; Viot G; Lungeanu A; Arghir A
    Psychiatry Res; 2012 May; 197(3):356-7. PubMed ID: 22365273
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 25.