These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
337 related articles for article (PubMed ID: 24361202)
1. 22q11.2 Microduplication in a patient with 19p13.12-13.13 deletion. Wang Y; Yu Y; Hu X; Li B; Qian J Gene; 2014 Mar; 537(1):164-8. PubMed ID: 24361202 [TBL] [Abstract][Full Text] [Related]
2. Molecular characterization of microduplication 22q11.2 in a girl with hypernasal speech. Soysal Y; Vermeesch J; Davani NA; Şensoy N; Hekimler K; İmirzalıoğlu N Genet Mol Res; 2011 Sep; 10(3):2148-54. PubMed ID: 21968682 [TBL] [Abstract][Full Text] [Related]
3. A 1.37-Mb 12p11.22-p11.21 deletion coincident with a 367-kb 22q11.2 duplication detected by array comparative genomic hybridization in an adolescent girl with autism and difficulty in self-care of menstruation. Chen CP; Lin SP; Chern SR; Wu PS; Su JW; Lee CC; Wang W Taiwan J Obstet Gynecol; 2014 Mar; 53(1):74-8. PubMed ID: 24767651 [TBL] [Abstract][Full Text] [Related]
4. 22q11.2 duplication syndrome: two new familial cases with some overlapping features with DiGeorge/velocardiofacial syndromes. Portnoï MF; Lebas F; Gruchy N; Ardalan A; Biran-Mucignat V; Malan V; Finkel L; Roger G; Ducrocq S; Gold F; Taillemite JL; Marlin S Am J Med Genet A; 2005 Aug; 137(1):47-51. PubMed ID: 16007629 [TBL] [Abstract][Full Text] [Related]
5. A unique phenotype in a patient with a rare triplication of the 22q11.2 region and new clinical insights of the 22q11.2 microduplication syndrome: a report of two cases. Vaz SO; Pires R; Pires LM; Carreira IM; Anjos R; Maciel P; Mota-Vieira L BMC Pediatr; 2015 Aug; 15():95. PubMed ID: 26297018 [TBL] [Abstract][Full Text] [Related]
6. CATCH 22 syndrome: report of 7 infants with follow-up data and review of the recent advancements in the genetic knowledge of the locus 22q11. Sergi C; Serpi M; Müller-Navia J; Schnabel PA; Hagl S; Otto HF; Ulmer HE Pathologica; 1999 Jun; 91(3):166-72. PubMed ID: 10536461 [TBL] [Abstract][Full Text] [Related]
7. 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]
8. Genomic findings in patients with clinical suspicion of 22q11.2 deletion syndrome. Koczkowska M; Wierzba J; Śmigiel R; Sąsiadek M; Cabała M; Ślężak R; Iliszko M; Kardaś I; Limon J; Lipska-Ziętkiewicz BS J Appl Genet; 2017 Feb; 58(1):93-98. PubMed ID: 27629806 [TBL] [Abstract][Full Text] [Related]
9. 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]
10. Falciform macular folds and chromosome 22q11.2: evidence in support of a locus for familial exudative vitreoretinopathy (FEVR). Gandhi JK; Tollefson TT; Telander DG Ophthalmic Genet; 2014 Jun; 35(2):112-6. PubMed ID: 23521024 [TBL] [Abstract][Full Text] [Related]
11. Newborn infant with inherited ring and de novo interstitial deletion on homologous chromosome 22s. Wenger SL; Boone LY; Cummins JH; Del Vecchio MA; Bay CA; Hummel M; Mowery-Rushton PA Am J Med Genet; 2000 Apr; 91(5):351-4. PubMed ID: 10766997 [TBL] [Abstract][Full Text] [Related]
12. A new genomic duplication syndrome complementary to the velocardiofacial (22q11 deletion) syndrome. Hassed SJ; Hopcus-Niccum D; Zhang L; Li S; Mulvihill JJ Clin Genet; 2004 May; 65(5):400-4. PubMed ID: 15099348 [TBL] [Abstract][Full Text] [Related]
13. 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]
14. A unique combination of 17pter trisomy and 21qter monosomy in a boy with developmental delay, severe intellectual disability, growth retardation and dysmorphisms. Zheng Z; Yao RE; Geng J; Jin X; Shen Y; Ying D; Fu Q; Yu Y Gene; 2013 Mar; 516(2):301-6. PubMed ID: 23296059 [TBL] [Abstract][Full Text] [Related]
15. Clinical and molecular description of the prenatal diagnosis of a fetus with a maternally inherited microduplication 22q11.2 of 2.5 Mb. Christopoulou G; Sismani C; Sakellariou M; Saklamaki M; Athanassiou V; Velissariou V Gene; 2013 Sep; 527(2):694-7. PubMed ID: 23506827 [TBL] [Abstract][Full Text] [Related]
16. 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]
17. An atypical 0.8 Mb inherited duplication of 22q11.2 associated with psychomotor impairment. Pebrel-Richard C; Kemeny S; Gouas L; Eymard-Pierre E; Blanc N; Francannet C; Tchirkov A; Goumy C; Vago P Eur J Med Genet; 2012 Nov; 55(11):650-5. PubMed ID: 22796526 [TBL] [Abstract][Full Text] [Related]
18. 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]
19. A complex submicroscopic chromosomal imbalance in 19p13.11 with one microduplication and two microtriplications. Thienpont B; Breckpot J; Vermeesch JR; Gewillig M; Devriendt K Eur J Med Genet; 2008; 51(3):219-25. PubMed ID: 18282819 [TBL] [Abstract][Full Text] [Related]