These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

155 related articles for article (PubMed ID: 37258294)

  • 1. The Subtlety of 22q11.2 Deletion Syndrome in a Preterm Neonate.
    Cline L; Aranda P; Jnah A
    Neonatal Netw; 2023 Jun; 42(3):137-144. PubMed ID: 37258294
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Anatomic patterns of conotruncal defects associated with deletion 22q11.
    Marino B; Digilio MC; Toscano A; Anaclerio S; Giannotti A; Feltri C; de Ioris MA; Angioni A; Dallapiccola B
    Genet Med; 2001; 3(1):45-8. PubMed ID: 11339377
    [TBL] [Abstract][Full Text] [Related]  

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

  • 4. A case of 22q11.2 deletion syndrome with right microphthalmia and left corneal staphyloma.
    Tarlan B; Kiratli H; Kılıç E; Utine E; Boduroğlu K
    Ophthalmic Genet; 2014 Dec; 35(4):248-51. PubMed ID: 23834556
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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; 14(1):35-42. PubMed ID: 18636635
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Importance of microdeletions of chromosomal region 22q11 as a cause of selected malformations of the ventricular outflow tracts and aortic arch: a three-year prospective study.
    Webber SA; Hatchwell E; Barber JC; Daubeney PE; Crolla JA; Salmon AP; Keeton BR; Temple IK; Dennis NR
    J Pediatr; 1996 Jul; 129(1):26-32. PubMed ID: 8757559
    [TBL] [Abstract][Full Text] [Related]  

  • 7. DiGeorge syndrome with isolated aortic coarctation and isolated ventricular septal defect in three sibs with a 22q11 deletion of maternal origin.
    Wilson DI; Cross IE; Goodship JA; Coulthard S; Carey AH; Scambler PJ; Bain HH; Hunter AS; Carter PE; Burn J
    Br Heart J; 1991 Oct; 66(4):308-12. PubMed ID: 1747284
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Frequency of 22q11 deletions in patients with conotruncal defects.
    Goldmuntz E; Clark BJ; Mitchell LE; Jawad AF; Cuneo BF; Reed L; McDonald-McGinn D; Chien P; Feuer J; Zackai EH; Emanuel BS; Driscoll DA
    J Am Coll Cardiol; 1998 Aug; 32(2):492-8. PubMed ID: 9708481
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Interruption of the aortic arch at the isthmus with DiGeorge syndrome and 22q11.2 deletion.
    Takahashi K; Kuwahara T; Nagatsu M
    Cardiol Young; 1999 Sep; 9(5):516-8. PubMed ID: 10535835
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Frequency of 22q11.2 microdeletion in children with congenital heart defects in western poland.
    Wozniak A; Wolnik-Brzozowska D; Wisniewska M; Glazar R; Materna-Kiryluk A; Moszura T; Badura-Stronka M; Skolozdrzy J; Krawczynski MR; Zeyland J; Bobkowski W; Slomski R; Latos-Bielenska A; Siwinska A
    BMC Pediatr; 2010 Dec; 10():88. PubMed ID: 21134246
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Isolated innominate artery in 22q11 microdeletion.
    Duke C; Chan KC
    Pediatr Cardiol; 2001; 22(1):80-2. PubMed ID: 11123139
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A unique phenotype in a patient with a rare triplication of the 22q11.2 region and new clinical insights of the 22q11.2 microduplication syndrome: a report of two cases.
    Vaz SO; Pires R; Pires LM; Carreira IM; Anjos R; Maciel P; Mota-Vieira L
    BMC Pediatr; 2015 Aug; 15():95. PubMed ID: 26297018
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Chromosome 22q11.2 Deletion Syndrome: A Comprehensive Review of Molecular Genetics in the Context of Multidisciplinary Clinical Approach.
    Szczawińska-Popłonyk A; Schwartzmann E; Chmara Z; Głukowska A; Krysa T; Majchrzycki M; Olejnicki M; Ostrowska P; Babik J
    Int J Mol Sci; 2023 May; 24(9):. PubMed ID: 37176024
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Prenatal diagnosis and molecular cytogenetic characterization of chromosome 22q11.2 deletion syndrome associated with congenital heart defects.
    Kuo YL; Chen CP; Wang LK; Ko TM; Chang TY; Chern SR; Wu PS; Chen YT; Chang SY
    Taiwan J Obstet Gynecol; 2014 Jun; 53(2):248-51. PubMed ID: 25017279
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Chromosome 22q11 deletions in patients with conotruncal heart defects.
    Khositseth A; Tocharoentanaphol C; Khowsathit P; Ruangdaraganon N
    Pediatr Cardiol; 2005; 26(5):570-3. PubMed ID: 16132309
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. The genetic implication for preceding generations of the prenatal diagnosis of interrupted aortic arch in association with unsuspected DiGeorge anomaly.
    Puder KS; Humes RA; Gold RL; Bawle EV; Goyert GL
    Am J Obstet Gynecol; 1995 Jul; 173(1):239-41. PubMed ID: 7631695
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Family studies in chromosome 22q11 deletion: further demonstration of phenotypic heterogeneity.
    De Silva D; Duffty P; Booth P; Auchterlonie I; Morrison N; Dean JC
    Clin Dysmorphol; 1995 Oct; 4(4):294-303. PubMed ID: 8574419
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Chromosome 22q11.2 deletion syndrome (DiGeorge and velocardiofacial syndromes).
    Perez E; Sullivan KE
    Curr Opin Pediatr; 2002 Dec; 14(6):678-83. PubMed ID: 12436034
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.