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Results by year

Year	Number of Results
1975	8
1976	2
1977	2
1978	4
1979	2
1980	4
1981	9
1982	5
1983	6
1984	11
1985	9
1986	8
1987	9
1988	7
1989	16
1990	5
1991	13
1992	14
1993	37
1994	17
1995	32
1996	44
1997	56
1998	47
1999	65
2000	46
2001	60
2002	48
2003	56
2004	45
2005	71
2006	91
2007	91
2008	91
2009	89
2010	99
2011	107
2012	102
2013	124
2014	137
2015	131
2016	119
2017	155
2018	158
2019	160
2020	158
2021	155
2022	152
2023	144
2024	46

2,711 results

Page of 272

Results by year

Page 1

Prenatal cardiac findings and 22q11.2 deletion syndrome: Fetal detection and evaluation.

Goldmuntz E, Bassett AS, Boot E, Marino B, Moldenhauer JS, Óskarsdóttir S, Putotto C, Rychik J, Schindewolf E, McDonald-McGinn DM, Blagowidow N. Goldmuntz E, et al. Prenat Diagn. 2024 Apr 9. doi: 10.1002/pd.6566. Online ahead of print. Prenat Diagn. 2024. PMID: 38593251 Review.

Outcomes of primary repair of cleft palate using sommerled intravelar veloplasty associated with velocardiofacial syndrome.

Esmailzade Moghimi S, Rezaei P, Sadeghi S, Feizi A, Derakhshandeh F. Esmailzade Moghimi S, et al. Int J Pediatr Otorhinolaryngol. 2024 Apr;179:111940. doi: 10.1016/j.ijporl.2024.111940. Epub 2024 Apr 2. Int J Pediatr Otorhinolaryngol. 2024. PMID: 38588634

Variants in Candidate Genes for Phenotype Heterogeneity in Patients with the 22q11.2 Deletion Syndrome.

Nunes N, Carvalho Nunes B, Zamariolli M, Cordeiro de Queiroz Soares D, Caires Dos Santos L, Gollo Dantas A, Ayres Meloni V, Iole Belangero S, Gil-Da-Silva-Lopes VL, Ae Kim C, Melaragno MI. Nunes N, et al. Genet Res (Camb). 2024 Mar 30;2024:5549592. doi: 10.1155/2024/5549592. eCollection 2024. Genet Res (Camb). 2024. PMID: 38586596 Free PMC article.

Synaptic-dependent developmental dysconnectivity in 22q11.2 deletion syndrome.

Alvino FG, Gini S, Minetti A, Pagani M, Sastre-Yagüe D, Barsotti N, De Guzman E, Schleifer C, Stuefer A, Kushan L, Montani C, Galbusera A, Papaleo F, Lombardo MV, Pasqualetti M, Bearden CE, Gozzi A. Alvino FG, et al. bioRxiv [Preprint]. 2024 Apr 3:2024.03.29.587339. doi: 10.1101/2024.03.29.587339. bioRxiv. 2024. PMID: 38585897 Free PMC article. Preprint.

DGS1 improves rice disease resistance by elevating pathogen-associated molecular pattern-triggered immunity.

Wang Y, Zheng C, Peng YL, Chen Q. Wang Y, et al. aBIOTECH. 2024 Feb 6;5(1):46-51. doi: 10.1007/s42994-024-00137-9. eCollection 2024 Mar. aBIOTECH. 2024. PMID: 38576430 Free PMC article.

Multiple paralogues and recombination mechanisms drive the high incidence of 22q11.2 Deletion Syndrome.

Vervoort L, Dierckxsens N, Santos MS, Meynants S, Souche E, Cools R, Heung T, Devriendt K, Peeters H, McDonald-McGinn DM, Swillen A, Breckpot J, Emanuel BS, Van Esch H, Bassett AS, Vermeesch JR. Vervoort L, et al. bioRxiv [Preprint]. 2024 Mar 18:2024.03.14.585046. doi: 10.1101/2024.03.14.585046. bioRxiv. 2024. PMID: 38562770 Free PMC article. Preprint.

The Outcomes of Cardiac Surgery in Children With DiGeorge Syndrome in a Single Center Experience: A Retrospective Cohort Study.

AlAshgar TM, AlDawsari NH, AlSanea NY, AlSalamah NA, AlSugair NS, Ardah HI, Kabbani MS. AlAshgar TM, et al. Cureus. 2024 Feb 28;16(2):e55186. doi: 10.7759/cureus.55186. eCollection 2024 Feb. Cureus. 2024. PMID: 38562270 Free PMC article.

Understanding the Variability of 22q11.2 Deletion Syndrome: The Role of Epigenetic Factors.

Cillo F, Coppola E, Habetswallner F, Cecere F, Pignata L, Toriello E, De Rosa A, Grilli L, Ammendola A, Salerno P, Romano R, Cirillo E, Merla G, Riccio A, Pignata C, Giardino G. Cillo F, et al. Genes (Basel). 2024 Feb 29;15(3):321. doi: 10.3390/genes15030321. Genes (Basel). 2024. PMID: 38540380 Free PMC article. Review.

Congenital cytomegalovirus infection in a preterm infant with 22q11.2 deletion syndrome and immunological abnormalities.

Shitara Y, Toyofuku E, Doi H, Mukai T, Kashima K, Kakiuchi S, Kato M, Takahashi N. Shitara Y, et al. Nagoya J Med Sci. 2024 Feb;86(1):149-154. doi: 10.18999/nagjms.86.1.149. Nagoya J Med Sci. 2024. PMID: 38505727 Free PMC article.

Social skills in neurodevelopmental disorders: a study using role-plays to assess adolescents and young adults with 22q11.2 deletion syndrome and autism spectrum disorders.

Feller C, Ilen L, Eliez S, Schneider M. Feller C, et al. J Neurodev Disord. 2024 Mar 18;16(1):11. doi: 10.1186/s11689-024-09527-y. J Neurodev Disord. 2024. PMID: 38500028 Free article.

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