BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

238 related articles for article (PubMed ID: 8574419)

  • 21. 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]  

  • 22. 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]  

  • 23. 22q11.2 deletion detected by
    Ramírez-Velazco A; Rivera H; Vásquez-Velázquez AI; Aguayo-Orozco TA; Delgadillo-Pérez S; Domínguez MG
    Colomb Med (Cali); 2018 Sep; 49(3):219-222. PubMed ID: 30410196
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Prevalence of 22q11 microdeletions in DiGeorge and velocardiofacial syndromes: implications for genetic counselling and prenatal diagnosis.
    Driscoll DA; Salvin J; Sellinger B; Budarf ML; McDonald-McGinn DM; Zackai EH; Emanuel BS
    J Med Genet; 1993 Oct; 30(10):813-7. PubMed ID: 8230155
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [Microdeletion 22q11.2. A too rarely diagnosed genetic change in psychiatric illnesses].
    Leyhe T; Haarmeier T; Dufke A; Giedke H
    Nervenarzt; 2002 May; 73(5):452-7. PubMed ID: 12078024
    [TBL] [Abstract][Full Text] [Related]  

  • 26. The 22q11.2 deletion syndrome.
    Yamagishi H
    Keio J Med; 2002 Jun; 51(2):77-88. PubMed ID: 12125909
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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]  

  • 28. DiGeorge syndrome/velocardiofacial syndrome: the chromosome 22q11.2 deletion syndrome.
    Sullivan KE
    Adv Exp Med Biol; 2007; 601():37-49. PubMed ID: 17712990
    [TBL] [Abstract][Full Text] [Related]  

  • 29. CATCH 22: deletion of locus 22q11 in velocardiofacial syndrome, DiGeorge anomaly, and nonsyndromic conotruncal defects.
    Hou JW; Wang JK; Tsai WY; Chou CC; Wang TR
    J Formos Med Assoc; 1997 Jun; 96(6):419-23. PubMed ID: 9216164
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Craniosynostosis: another feature of the 22q11.2 deletion syndrome.
    McDonald-McGinn DM; Gripp KW; Kirschner RE; Maisenbacher MK; Hustead V; Schauer GM; Keppler-Noreuil KM; Ciprero KL; Pasquariello P; LaRossa D; Bartlett SP; Whitaker LA; Zackai EH
    Am J Med Genet A; 2005 Aug; 136A(4):358-62. PubMed ID: 16001439
    [TBL] [Abstract][Full Text] [Related]  

  • 31. DNA fluorescent probes for diagnosis of velocardiofacial and related syndromes.
    Crifasi PA; Michels VV; Driscoll DJ; Jalal SM; Dewald GW
    Mayo Clin Proc; 1995 Dec; 70(12):1148-53. PubMed ID: 7490915
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Submicroscopic deletion in chromosome 22q11 in trizygous triplet siblings and their father. Clinical variability of 22q11 deletion.
    Devriendt K; Van Hoestenberghe R; Van Hole C; Devlieger H; Gewillig M; Moerman P; Van den Berghe H; Fryns JP
    Clin Genet; 1997 Apr; 51(4):246-9. PubMed ID: 9184246
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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]  

  • 34. 3 generation pedigree with paternal transmission of the 22q11.2 deletion syndrome: Intrafamilial phenotypic variability.
    Vergaelen E; Swillen A; Van Esch H; Claes S; Van Goethem G; Devriendt K
    Eur J Med Genet; 2015 Apr; 58(4):244-8. PubMed ID: 25655469
    [TBL] [Abstract][Full Text] [Related]  

  • 35. 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]  

  • 36. Congenital diaphragmatic hernia in 22q11.2 deletion syndrome.
    Unolt M; DiCairano L; Schlechtweg K; Barry J; Howell L; Kasperski S; Nance M; Adzick NS; Zackai EH; McDonald-McGinn DM
    Am J Med Genet A; 2017 Jan; 173(1):135-142. PubMed ID: 27682988
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Genomic findings in patients with clinical suspicion of 22q11.2 deletion syndrome.
    Koczkowska M; Wierzba J; Śmigiel R; Sąsiadek M; Cabała M; Ślężak R; Iliszko M; Kardaś I; Limon J; Lipska-Ziętkiewicz BS
    J Appl Genet; 2017 Feb; 58(1):93-98. PubMed ID: 27629806
    [TBL] [Abstract][Full Text] [Related]  

  • 38. A population-based study of the 22q11.2 deletion: phenotype, incidence, and contribution to major birth defects in the population.
    Botto LD; May K; Fernhoff PM; Correa A; Coleman K; Rasmussen SA; Merritt RK; O'Leary LA; Wong LY; Elixson EM; Mahle WT; Campbell RM
    Pediatrics; 2003 Jul; 112(1 Pt 1):101-7. PubMed ID: 12837874
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [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]  

  • 40. 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]  

    [Previous]   [Next]    [New Search]
    of 12.