234 related articles for article (PubMed ID: 22051516)
1. Sex differences in reproductive fitness contribute to preferential maternal transmission of 22q11.2 deletions.
Costain G; Chow EW; Silversides CK; Bassett AS
J Med Genet; 2011 Dec; 48(12):819-24. PubMed ID: 22051516
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. All-cause mortality and survival in adults with 22q11.2 deletion syndrome.
Van L; Heung T; Graffi J; Ng E; Malecki S; Van Mil S; Boot E; Corral M; Chow EWC; Hodgkinson KA; Silversides C; Bassett AS
Genet Med; 2019 Oct; 21(10):2328-2335. PubMed ID: 30948858
[TBL] [Abstract][Full Text] [Related]
5. [Neurocognitive and psychiatric management of the 22q11.2 deletion syndrome].
Demily C; Rossi M; Schneider M; Edery P; Leleu A; d'Amato T; Franck N; Eliez S
Encephale; 2015 Jun; 41(3):266-73. PubMed ID: 25523123
[TBL] [Abstract][Full Text] [Related]
6. Differences in speech and language abilities between children with 22q11.2 deletion syndrome and children with phenotypic features of 22q11.2 deletion syndrome but without microdeletion.
Rakonjac M; Cuturilo G; Stevanovic M; Jelicic L; Subotic M; Jovanovic I; Drakulic D
Res Dev Disabil; 2016 Aug; 55():322-9. PubMed ID: 27235769
[TBL] [Abstract][Full Text] [Related]
7. 3 generation pedigree with paternal transmission of the 22q11.2 deletion syndrome: Intrafamilial phenotypic variability.
Vergaelen E; Swillen A; Van Esch H; Claes S; Van Goethem G; Devriendt K
Eur J Med Genet; 2015 Apr; 58(4):244-8. PubMed ID: 25655469
[TBL] [Abstract][Full Text] [Related]
8. Congenital heart defects and chromosomal anomalies including 22q11 microdeletion (CATCH 22).
Soares G; Alvares S; Rocha C; Teixeira MF; Mota MC; Reis MI; Feijó MJ; Lima MR; Pinto MR
Rev Port Cardiol; 2005 Mar; 24(3):349-71. PubMed ID: 15929620
[TBL] [Abstract][Full Text] [Related]
9. Reproductive Outcomes in Adults with 22q11.2 Deletion Syndrome.
Palmer LD; McManus Z; Heung T; McAlpine G; Blagojevic C; Corral M; Bassett AS
Genes (Basel); 2022 Nov; 13(11):. PubMed ID: 36421801
[TBL] [Abstract][Full Text] [Related]
10. 22q11.2DS deletion syndrome: developmental milestones in infants and toddlers.
Roizen NJ; Antshel KM; Fremont W; AbdulSabur N; Higgins AM; Shprintzen RJ; Kates WR
J Dev Behav Pediatr; 2007 Apr; 28(2):119-24. PubMed ID: 17435462
[TBL] [Abstract][Full Text] [Related]
11. Reproductive Health Issues for Adults with a Common Genomic Disorder: 22q11.2 Deletion Syndrome.
Chan C; Costain G; Ogura L; Silversides CK; Chow EW; Bassett AS
J Genet Couns; 2015 Oct; 24(5):810-21. PubMed ID: 25579115
[TBL] [Abstract][Full Text] [Related]
12. Prevalence and clinical manifestations of 22q11.2 microdeletion in adults with selected conotruncal anomalies.
Beauchesne LM; Warnes CA; Connolly HM; Ammash NM; Grogan M; Jalal SM; Michels VV
J Am Coll Cardiol; 2005 Feb; 45(4):595-8. PubMed ID: 15708709
[TBL] [Abstract][Full Text] [Related]
13. [Microdeletion 22q11: apropos of case of schizophrenia in an adolescent].
Pinquier C; Héron D; de Carvalho W; Lazar G; Mazet P; Cohen D
Encephale; 2001; 27(1):45-50. PubMed ID: 11294038
[TBL] [Abstract][Full Text] [Related]
14. Differential gene expression in the hippocampus of the Df1/+ mice: a model for 22q11.2 deletion syndrome and schizophrenia.
Sivagnanasundaram S; Fletcher D; Hubank M; Illingworth E; Skuse D; Scambler P
Brain Res; 2007 Mar; 1139():48-59. PubMed ID: 17292336
[TBL] [Abstract][Full Text] [Related]
15. Prospective control abilities during visuo-manual tracking in children with 22q11.2 Deletion syndrome compared to age- and IQ-matched controls.
Van Aken K; Swillen A; Beirinckx M; Janssens L; Caeyenberghs K; Smits-Engelsman B
Res Dev Disabil; 2010; 31(3):634-41. PubMed ID: 20181458
[TBL] [Abstract][Full Text] [Related]
16. [Detection and related analysis to chromosome 22q11 microdeletion in patients with congenital heart diseases].
Xu ZF; Yi L; Mo XM; Hu Y; Wang DJ; Zhu RF; Jiang YZ; Wu X; Wu Z; Shen L; Zhang Y; Zhong XL
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2006 Jun; 23(3):250-5. PubMed ID: 16767657
[TBL] [Abstract][Full Text] [Related]
17. Predominant negative symptoms in 22q11.2 deletion syndrome and their associations with cognitive functioning and functional outcome.
Schneider M; Van der Linden M; Menghetti S; Glaser B; Debbané M; Eliez S
J Psychiatr Res; 2014 Jan; 48(1):86-93. PubMed ID: 24189154
[TBL] [Abstract][Full Text] [Related]
18. Complete Sequence of the 22q11.2 Allele in 1,053 Subjects with 22q11.2 Deletion Syndrome Reveals Modifiers of Conotruncal Heart Defects.
Zhao Y; Diacou A; Johnston HR; Musfee FI; McDonald-McGinn DM; McGinn D; Crowley TB; Repetto GM; Swillen A; Breckpot J; Vermeesch JR; Kates WR; Digilio MC; Unolt M; Marino B; Pontillo M; Armando M; Di Fabio F; Vicari S; van den Bree M; Moss H; Owen MJ; Murphy KC; Murphy CM; Murphy D; Schoch K; Shashi V; Tassone F; Simon TJ; Shprintzen RJ; Campbell L; Philip N; Heine-Suñer D; García-Miñaúr S; Fernández L; ; Bearden CE; Vingerhoets C; van Amelsvoort T; Eliez S; Schneider M; Vorstman JAS; Gothelf D; Zackai E; Agopian AJ; Gur RE; Bassett AS; Emanuel BS; Goldmuntz E; Mitchell LE; Wang T; Morrow BE
Am J Hum Genet; 2020 Jan; 106(1):26-40. PubMed ID: 31870554
[TBL] [Abstract][Full Text] [Related]
19. Subtelomeric rearrangements and 22q11.2 deletion syndrome in anomalous growth-restricted fetuses with normal or balanced G-banded karyotype.
Chen M; Hwu WL; Kuo SJ; Chen CP; Yin PL; Chang SP; Lee DJ; Chen TH; Wang BT; Lin CC
Ultrasound Obstet Gynecol; 2006 Dec; 28(7):939-43. PubMed ID: 17121426
[TBL] [Abstract][Full Text] [Related]
20. Incidences of micro-deletion/duplication 22q11.2 detected by multiplex ligation-dependent probe amplification in patients with congenital cardiac disease who are scheduled for cardiac surgery.
Hu Y; Zhu X; Yang Y; Mo X; Sheng M; Yao J; Wang D
Cardiol Young; 2009 Apr; 19(2):179-84. PubMed ID: 19224675
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
