242 related articles for article (PubMed ID: 22365273)
41. Is the autosomal dominant Optiz GBBB syndrome part of the DiGeorge/velocardiofacial syndrome with deletions of chromosome area 22q11.2?
Wulfsberg EA
Am J Med Genet; 1996 Aug; 64(3):523-4. PubMed ID: 8862634
[No Abstract] [Full Text] [Related]
42. Genetic dosage compensation in a family with velo-cardio-facial/DiGeorge/22q11.2 deletion syndrome.
Alkalay AA; Guo T; Montagna C; Digilio MC; Dallapiccola B; Marino B; Morrow B
Am J Med Genet A; 2011 Mar; 155A(3):548-54. PubMed ID: 21337693
[TBL] [Abstract][Full Text] [Related]
43. [Diagnosis of 22q11.2 deletion syndrome in the context of newly developed psychosis].
Kaltenboeck A; Friedrich F; Hinterbuchinger B; Litvan Z; Mossaheb N
Neuropsychiatr; 2016 Dec; 30(4):223-226. PubMed ID: 27822729
[TBL] [Abstract][Full Text] [Related]
44. Microsatellite DNA markers detects 95% of chromosome 22q11 deletions.
Bonnet D; Cormier-Daire V; Kachaner J; Szezepanski I; Souillard P; Sidi D; Munnich A; Lyonnet S
Am J Med Genet; 1997 Jan; 68(2):182-4. PubMed ID: 9028455
[TBL] [Abstract][Full Text] [Related]
45. DiGeorge syndrome: new insights.
Goldmuntz E
Clin Perinatol; 2005 Dec; 32(4):963-78, ix-x. PubMed ID: 16325672
[TBL] [Abstract][Full Text] [Related]
46. 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]
47. [Partial DiGeorge syndrome caused by 22q11.2 typical microdeletion without cardiac defect: report of two cases].
He JX; Zhang S; Han TL; Yu FH; Liu XY; Xu BP; Shen KL; Jiang ZF
Zhongguo Dang Dai Er Ke Za Zhi; 2014 May; 16(5):541-3. PubMed ID: 24857009
[No Abstract] [Full Text] [Related]
48. 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]
49. 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]
50. Atypical microdeletion 22q11.2 in a patient with tetralogy of Fallot.
Carli D; Moroni A; Eleonora DG; Zonta A; Montin D; Licciardi F; Aidala E; Bordese R; Carlo PN; Brusco A; Giovanni Battista F; Mussa A
J Genet; 2021; 100():. PubMed ID: 33707356
[TBL] [Abstract][Full Text] [Related]
51. Pachygyria, seizures, hypotonia, and growth retardation in a patient with an atypical 1.33Mb inherited microduplication at 22q11.23.
Chang J; Zhao L; Chen C; Peng Y; Xia Y; Tang G; Bai T; Zhang Y; Ma R; Guo R; Mei L; Liang D; Cao Q; Wu L
Gene; 2015 Sep; 569(1):46-50. PubMed ID: 26099517
[TBL] [Abstract][Full Text] [Related]
52. The Identification of Microdeletion and Reciprocal Microduplication in 22q11.2 Using High-Resolution CMA Technology.
Leite AJ; Pinto IP; Cunha DM; Ribeiro CL; da Silva CC; da Cruz AD; Minasi LB
Biomed Res Int; 2016; 2016():7415438. PubMed ID: 27123452
[TBL] [Abstract][Full Text] [Related]
53. 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]
54. Recognizing a common genetic syndrome: 22q11.2 deletion syndrome.
Kapadia RK; Bassett AS
CMAJ; 2008 Feb; 178(4):391-3. PubMed ID: 18268261
[No Abstract] [Full Text] [Related]
55. Consequences of 22q11.2 Microdeletion on the Genome, Individual and Population Levels.
Karbarz M
Genes (Basel); 2020 Aug; 11(9):. PubMed ID: 32842603
[TBL] [Abstract][Full Text] [Related]
56. Primary amenorrhea and absent uterus in the 22q11.2 deletion syndrome.
Sundaram UT; McDonald-McGinn DM; Huff D; Emanuel BS; Zackai EH; Driscoll DA; Bodurtha J
Am J Med Genet A; 2007 Sep; 143A(17):2016-8. PubMed ID: 17676598
[TBL] [Abstract][Full Text] [Related]
57. [Molecular basis of microdeletion 22q11].
Bouvagnet P
Arch Pediatr; 2002 May; 9 Suppl 2():97s-99s. PubMed ID: 12108307
[No Abstract] [Full Text] [Related]
58. Genomic disorders on chromosome 22.
Yu S; Graf WD; Shprintzen RJ
Curr Opin Pediatr; 2012 Dec; 24(6):665-71. PubMed ID: 23111679
[TBL] [Abstract][Full Text] [Related]
59. The chromosome 22q11.2 deletion: from the unification of biomedical fields to a new kind of genetic condition.
Navon D; Shwed U
Soc Sci Med; 2012 Nov; 75(9):1633-41. PubMed ID: 22871261
[TBL] [Abstract][Full Text] [Related]
60. Mapping the deletion endpoints in individuals with 22q11.2 deletion syndrome by droplet digital PCR.
Hwang VJ; Maar D; Regan J; Angkustsiri K; Simon TJ; Tassone F
BMC Med Genet; 2014 Oct; 15():106. PubMed ID: 25312060
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
