BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

205 related articles for article (PubMed ID: 12605524)

  • 1. Is isolated palatal anomaly an indication to screen for 22q11 region deletion?
    Reish O; Finkelstein Y; Mesterman R; Nachmani A; Wolach B; Fejgin M; Amiel A
    Cleft Palate Craniofac J; 2003 Mar; 40(2):176-9. PubMed ID: 12605524
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Videonasopharyngoscopy in patients with 22q11.2 deletion syndrome (Shprintzen syndrome).
    Ysunza A; Pamplona MC; Ramírez E; Canún S; Sierra MC; Silva-Rojas A
    Int J Pediatr Otorhinolaryngol; 2003 Aug; 67(8):911-5. PubMed ID: 12880672
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Detection of a 22q11.2 deletion in cardiac patients suggests a risk for velopharyngeal incompetence.
    McDonald-McGinn DM; Driscoll DA; Emanuel BS; Goldmuntz E; Clark BJ; Solot C; Cohen M; Schultz P; LaRossa D; Randall P; Zackai EH
    Pediatrics; 1997 May; 99(5):E9. PubMed ID: 9113966
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Screening of patients at risk for 22q11 deletion.
    Barisić I; Morozin Pohovski L; Petković I; Cvetko Z; Stipancić G; Bagatin M
    Coll Antropol; 2008 Mar; 32(1):165-9. PubMed ID: 18494202
    [TBL] [Abstract][Full Text] [Related]  

  • 6. No justification of routine screening for 22q11 deletions in patients with overt cleft palate.
    Ruiter EM; Bongers EM; Smeets D; Kuijpers-Jagtman AM; Hamel BC
    Clin Genet; 2003 Sep; 64(3):216-9. PubMed ID: 12919136
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Clinical features in 130 patients with the velo-cardio-facial syndrome. The Leuven experience.
    Vantrappen G; Rommel N; Devriendt K; Cremers CW; Feenstra L; Fryns JP
    Acta Otorhinolaryngol Belg; 2001; 55(1):43-8. PubMed ID: 11256191
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The search for hemizygosity at 22qll in patients with isolated cleft palate.
    Mingarelli R; Digilio MC; Mari A; Amati F; Standoli L; Giannotti A; Novelli G; Dallapiccola B
    J Craniofac Genet Dev Biol; 1996; 16(2):118-21. PubMed ID: 8773902
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Clinical Features in Patients With 22q11.2 Deletion Syndrome Ascertained by Palatal Abnormalities.
    Vieira TP; Monteiro FP; Sgardioli IC; Souza J; Fett-Conte AC; Monlleó IL; Fontes MB; Félix TM; Leal GF; Ribeiro EM; Gil-da-Silva-Lopes VL
    Cleft Palate Craniofac J; 2015 Jul; 52(4):411-6. PubMed ID: 24805874
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. 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]  

  • 12. Palate abnormalities in Chilean patients with chromosome 22q11 microdeletion syndrome.
    Lay-Son G; Palomares M; Guzman ML; Vasquez M; Puga A; Repetto GM
    Int J Pediatr Otorhinolaryngol; 2012 Dec; 76(12):1726-8. PubMed ID: 22939891
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Psychiatric inpatients and chromosome deletions within 22q11.2.
    Sugama S; Namihira T; Matsuoka R; Taira N; Eto Y; Maekawa K
    J Neurol Neurosurg Psychiatry; 1999 Dec; 67(6):803-6. PubMed ID: 10567504
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Velo-cardio-facial syndrome: frequency and extent of 22q11 deletions.
    Lindsay EA; Goldberg R; Jurecic V; Morrow B; Carlson C; Kucherlapati RS; Shprintzen RJ; Baldini A
    Am J Med Genet; 1995 Jul; 57(3):514-22. PubMed ID: 7677167
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Chromosome 22q11 deletion and other chromosome aberrations in cases with cleft palate, congenital heart defects and/or mental disability. A survey based on the Danish Facial Cleft Register.
    Brøndum-Nielsen K; Christensen K
    Clin Genet; 1996 Sep; 50(3):116-20. PubMed ID: 8946108
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Microdeletions of chromosomal region 22q11 in patients with congenital conotruncal cardiac defects.
    Goldmuntz E; Driscoll D; Budarf ML; Zackai EH; McDonald-McGinn DM; Biegel JA; Emanuel BS
    J Med Genet; 1993 Oct; 30(10):807-12. PubMed ID: 7901419
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Under-recognition of 22q11.2 deletion in adult Chinese patients with conotruncal anomalies: implications in transitional care.
    Liu AP; Chow PC; Lee PP; Mok GT; Tang WF; Lau ET; Lam ST; Chan KY; Kan AS; Chau AK; Cheung YF; Lau YL; Chung BH
    Eur J Med Genet; 2014; 57(6):306-11. PubMed ID: 24721633
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Otolaryngological manifestations of velocardiofacial syndrome: a retrospective review of 35 patients.
    Ford LC; Sulprizio SL; Rasgon BM
    Laryngoscope; 2000 Mar; 110(3 Pt 1):362-7. PubMed ID: 10718420
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Presence of 22q11 deletion in postadenoidectomy velopharyngeal insufficiency.
    Perkins JA; Sie K; Gray S
    Arch Otolaryngol Head Neck Surg; 2000 May; 126(5):645-8. PubMed ID: 10807333
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.