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2. 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]
3. Prevalence of duplications and deletions of the 22q11 DiGeorge syndrome region in a population-based sample of infants with cleft palate. Sivertsen A; Lie RT; Wilcox AJ; Abyholm F; Vindenes H; Haukanes BI; Houge G Am J Med Genet A; 2007 Jan; 143A(2):129-34. PubMed ID: 17163526 [TBL] [Abstract][Full Text] [Related]
4. Identification of novel candidate genes associated with cleft lip and palate using array comparative genomic hybridisation. Osoegawa K; Vessere GM; Utami KH; Mansilla MA; Johnson MK; Riley BM; L'Heureux J; Pfundt R; Staaf J; van der Vliet WA; Lidral AC; Schoenmakers EF; Borg A; Schutte BC; Lammer EJ; Murray JC; de Jong PJ J Med Genet; 2008 Feb; 45(2):81-6. PubMed ID: 17873121 [TBL] [Abstract][Full Text] [Related]
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6. 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]
7. Labyrinthine malformation in the 22q11.2 deletion syndrome. Hopsu E; Markkola A; Pitkäranta A Clin Dysmorphol; 2007 Jan; 16(1):67-68. PubMed ID: 17159521 [TBL] [Abstract][Full Text] [Related]
8. 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]
13. Cleft palate in a patient with the nested 22q11.2 LCR C to D deletion. Williams CL; Nelson KR; Grant JH; Mikhail FM; Robin NH Am J Med Genet A; 2016 Jan; 170A(1):260-2. PubMed ID: 26419407 [No Abstract] [Full Text] [Related]
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15. 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]