784 related articles for article (PubMed ID: 26297018)
21. Microduplications in 22q11.2 and 8q22.1 associated with mild mental retardation and generalized overgrowth.
Tarsitano M; Ceglia C; Novelli A; Capalbo A; Lombardo B; Pastore L; Fioretti G; Vicari L; Pisanti MA; Friso P; Cavaliere ML
Gene; 2014 Feb; 536(1):213-6. PubMed ID: 24315824
[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. 22q11.2 Microduplication with thyroid hemiagenesis.
Kim HJ; Jo HS; Yoo EG; Chung IH; Kim SW; Lee KH; Chang YH
Horm Res Paediatr; 2013; 79(4):243-9. PubMed ID: 23364243
[TBL] [Abstract][Full Text] [Related]
24. Atypical 22q11.2 Microduplication with "Typical" Signs and Overgrowth.
Fischer M; Klopocki E
Cytogenet Genome Res; 2020; 160(11-12):659-663. PubMed ID: 33472199
[TBL] [Abstract][Full Text] [Related]
25. Ocular manifestations of 22q11.2 microduplication.
Cordovez JA; Capasso J; Lingao MD; Sadagopan KA; Spaeth GL; Wasserman BN; Levin AV
Ophthalmology; 2014 Jan; 121(1):392-398. PubMed ID: 23972321
[TBL] [Abstract][Full Text] [Related]
26. Lack of correlation between impaired T cell production, immunodeficiency, and other phenotypic features in chromosome 22q11.2 deletion syndromes.
Sullivan KE; Jawad AF; Randall P; Driscoll DA; Emanuel BS; McDonald-McGinn DM; Zackai EH
Clin Immunol Immunopathol; 1998 Feb; 86(2):141-6. PubMed ID: 9473376
[TBL] [Abstract][Full Text] [Related]
27. Confirmation that the conotruncal anomaly face syndrome is associated with a deletion within 22q11.2.
Matsuoka R; Takao A; Kimura M; Imamura S; Kondo C; Joh-o K; Ikeda K; Nishibatake M; Ando M; Momma K
Am J Med Genet; 1994 Nov; 53(3):285-9. PubMed ID: 7856665
[TBL] [Abstract][Full Text] [Related]
28. Genetic basis of DiGeorge and velocardiofacial syndromes.
Driscoll DA
Curr Opin Pediatr; 1994 Dec; 6(6):702-6. PubMed ID: 7849818
[TBL] [Abstract][Full Text] [Related]
29. De novo microduplication at 22q11.21 in a patient with VACTERL association.
Schramm C; Draaken M; Bartels E; Boemers TM; Aretz S; Brockschmidt FF; Nöthen MM; Ludwig M; Reutter H
Eur J Med Genet; 2011; 54(1):9-13. PubMed ID: 20849991
[TBL] [Abstract][Full Text] [Related]
30. 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]
31. The deletions of 22q11--the Portuguese experience.
Gaspar IM; Lourenço MT; Reis MI; Soares MA; Nogueira G; Ferreira F; Feijóo MJ
Genet Couns; 1999; 10(1):51-7. PubMed ID: 10191429
[TBL] [Abstract][Full Text] [Related]
32. [Congenital cardiovascular malformations and chromosome microdeletions in 22q11.2].
Trost D; Engels H; Bauriedel G; Wiebe W; Schwanitz G
Dtsch Med Wochenschr; 1999 Jan; 124(1-2):3-7. PubMed ID: 9951451
[TBL] [Abstract][Full Text] [Related]
33. 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]
34. Cardiac evaluation of patients with 22q11.2 duplication syndrome.
Butensky A; de Rinaldis CP; Patel S; Edman S; Bailey A; McGinn DE; Zackai E; Crowley TB; McDonald-McGinn DM; Min J; Goldmuntz E
Am J Med Genet A; 2021 Mar; 185(3):753-758. PubMed ID: 33369133
[TBL] [Abstract][Full Text] [Related]
35. 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]
36. Microduplication 22q11.2: a new chromosomal syndrome.
Portnoï MF
Eur J Med Genet; 2009; 52(2-3):88-93. PubMed ID: 19254783
[TBL] [Abstract][Full Text] [Related]
37. 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]
38. 22q11.2 duplications in a UK cohort with bladder exstrophy-epispadias complex.
Beaman GM; Woolf AS; Cervellione RM; Keene D; Mushtaq I; Urquhart JE; Stuart HM; Newman WG
Am J Med Genet A; 2019 Mar; 179(3):404-409. PubMed ID: 30628148
[TBL] [Abstract][Full Text] [Related]
39. Microdeletion of 22q11 (CATCH 22) in children with conotruncal heart defect and extracardiac malformations.
Alikaşifoğlu M; Malkoç N; Ceviz N; Ozme S; Uludoğan S; Tunçbilek E
Turk J Pediatr; 2000; 42(3):215-8. PubMed ID: 11105620
[TBL] [Abstract][Full Text] [Related]
40. Phenotypic discordance in monozygotic twins with 22q11.2 deletion.
Yamagishi H; Ishii C; Maeda J; Kojima Y; Matsuoka R; Kimura M; Takao A; Momma K; Matsuo N
Am J Med Genet; 1998 Jul; 78(4):319-21. PubMed ID: 9714432
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]