384 related articles for article (PubMed ID: 16512914)
21. AT-rich palindromes mediate the constitutional t(11;22) translocation.
Edelmann L; Spiteri E; Koren K; Pulijaal V; Bialer MG; Shanske A; Goldberg R; Morrow BE
Am J Hum Genet; 2001 Jan; 68(1):1-13. PubMed ID: 11095996
[TBL] [Abstract][Full Text] [Related]
22. Concurrent microdeletion and duplication of 22q11.2.
Blennow E; Lagerstedt K; Malmgren H; Sahlén S; Schoumans J; Anderlid B
Clin Genet; 2008 Jul; 74(1):61-7. PubMed ID: 18445048
[TBL] [Abstract][Full Text] [Related]
23. Atypical 22q11.2 deletion in a patient with DGS/VCFS spectrum.
Nogueira SI; Hacker AM; Bellucco FT; Christofolini DM; Kulikowski LD; Cernach MC; Emanuel BS; Melaragno MI
Eur J Med Genet; 2008; 51(3):226-30. PubMed ID: 18342595
[TBL] [Abstract][Full Text] [Related]
24. DiGeorge syndrome: new insights.
Goldmuntz E
Clin Perinatol; 2005 Dec; 32(4):963-78, ix-x. PubMed ID: 16325672
[TBL] [Abstract][Full Text] [Related]
25. Identification of novel deletions of 15q11q13 in Angelman syndrome by array-CGH: molecular characterization and genotype-phenotype correlations.
Sahoo T; Bacino CA; German JR; Shaw CA; Bird LM; Kimonis V; Anselm I; Waisbren S; Beaudet AL; Peters SU
Eur J Hum Genet; 2007 Sep; 15(9):943-9. PubMed ID: 17522620
[TBL] [Abstract][Full Text] [Related]
26. Cat eye syndrome chromosome breakpoint clustering: identification of two intervals also associated with 22q11 deletion syndrome breakpoints.
McTaggart KE; Budarf ML; Driscoll DA; Emanuel BS; Ferreira P; McDermid HE
Cytogenet Cell Genet; 1998; 81(3-4):222-8. PubMed ID: 9730608
[TBL] [Abstract][Full Text] [Related]
27. DiGeorge anomaly and chromosome 10p deletions: one or two loci?
Dasouki M; Jurecic V; Phillips JA; Whitlock JA; Baldini A
Am J Med Genet; 1997 Nov; 73(1):72-5. PubMed ID: 9375926
[TBL] [Abstract][Full Text] [Related]
28. Candidate genes and the behavioral phenotype in 22q11.2 deletion syndrome.
Prasad SE; Howley S; Murphy KC
Dev Disabil Res Rev; 2008; 14(1):26-34. PubMed ID: 18636634
[TBL] [Abstract][Full Text] [Related]
29. A novel Alu-mediated 61-kb deletion of the von Willebrand factor (VWF) gene whose breakpoints co-locate with putative matrix attachment regions.
Xie F; Wang X; Cooper DN; Chuzhanova N; Fang Y; Cai X; Wang Z; Wang H
Blood Cells Mol Dis; 2006; 36(3):385-91. PubMed ID: 16690331
[TBL] [Abstract][Full Text] [Related]
30. The 22q11.2 deletion syndrome.
Emanuel BS; McDonald-McGinn D; Saitta SC; Zackai EH
Adv Pediatr; 2001; 48():39-73. PubMed ID: 11480765
[TBL] [Abstract][Full Text] [Related]
31. Deletion 22q11: spectrum of associated disorders.
Hay BN
Semin Pediatr Neurol; 2007 Sep; 14(3):136-9. PubMed ID: 17980310
[TBL] [Abstract][Full Text] [Related]
32. Parental and chromosomal origins of microdeletion and duplication syndromes involving 7q11.23, 15q11-q13 and 22q11.
Thomas NS; Durkie M; Potts G; Sandford R; Van Zyl B; Youings S; Dennis NR; Jacobs PA
Eur J Hum Genet; 2006 Jul; 14(7):831-7. PubMed ID: 16617304
[TBL] [Abstract][Full Text] [Related]
33. A method for accurate detection of genomic microdeletions using real-time quantitative PCR.
Weksberg R; Hughes S; Moldovan L; Bassett AS; Chow EW; Squire JA
BMC Genomics; 2005 Dec; 6():180. PubMed ID: 16351727
[TBL] [Abstract][Full Text] [Related]
34. Low-copy repeats mediate the common 3-Mb deletion in patients with velo-cardio-facial syndrome.
Edelmann L; Pandita RK; Morrow BE
Am J Hum Genet; 1999 Apr; 64(4):1076-86. PubMed ID: 10090893
[TBL] [Abstract][Full Text] [Related]
35. 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]
36. A common molecular basis for rearrangement disorders on chromosome 22q11.
Edelmann L; Pandita RK; Spiteri E; Funke B; Goldberg R; Palanisamy N; Chaganti RS; Magenis E; Shprintzen RJ; Morrow BE
Hum Mol Genet; 1999 Jul; 8(7):1157-67. PubMed ID: 10369860
[TBL] [Abstract][Full Text] [Related]
37. Molecular and genetic aspects of DiGeorge/velocardiofacial syndrome.
Driscoll DA
Methods Mol Med; 2006; 126():43-55. PubMed ID: 16930005
[TBL] [Abstract][Full Text] [Related]
38. 1.5 Mb de novo 22q11.21 microduplication in a patient with cognitive deficits and dysmorphic facial features.
Alberti A; Romano C; Falco M; Calì F; Schinocca P; Galesi O; Spalletta A; Di Benedetto D; Fichera M
Clin Genet; 2007 Feb; 71(2):177-82. PubMed ID: 17250668
[TBL] [Abstract][Full Text] [Related]
39. A transcription map in the CATCH22 critical region: identification, mapping, and ordering of four novel transcripts expressed in heart.
Lindsay EA; Rizzu P; Antonacci R; Jurecic V; Delmas-Mata J; Lee CC; Kim UJ; Scambler PJ; Baldini A
Genomics; 1996 Feb; 32(1):104-12. PubMed ID: 8786095
[TBL] [Abstract][Full Text] [Related]
40. New tetranucleotide STRP markers for detecting the 22q11.2 deletion.
Yi L; Xu ZF; Mo XM; Hu YL; Wang DJ; Han B; Wang Y; Yang C; Jiang YZ; Shen L; Wu X; Zhu RF; Zhou XJ
Mol Cell Probes; 2006 Dec; 20(6):359-65. PubMed ID: 16774813
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]