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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1959 1
1960 2
1964 2
1965 3
1967 1
1968 3
1969 3
1971 2
1972 3
1973 2
1974 6
1975 9
1976 5
1977 20
1978 15
1979 16
1980 17
1981 20
1982 16
1983 22
1984 21
1985 20
1986 23
1987 15
1988 18
1989 32
1990 12
1991 24
1992 19
1993 46
1994 31
1995 51
1996 54
1997 75
1998 69
1999 87
2000 60
2001 77
2002 62
2003 64
2004 52
2005 90
2006 103
2007 104
2008 112
2009 102
2010 124
2011 129
2012 119
2013 159
2014 163
2015 156
2016 147
2017 176
2018 183
2019 190
2020 215
2021 179
2022 189
2023 175
2024 101

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3,563 results

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Page 1
Chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome).
McDonald-McGinn DM, Sullivan KE. McDonald-McGinn DM, et al. Medicine (Baltimore). 2011 Jan;90(1):1-18. doi: 10.1097/MD.0b013e3182060469. Medicine (Baltimore). 2011. PMID: 21200182 Free article. Review.
Chromosome 22q11.2 deletion syndrome is a common syndrome also known as DiGeorge syndrome and velocardiofacial syndrome. It occurs in approximately 1:4000 births, and the incidence is increasing due to affected parents bearing their own affected …
Chromosome 22q11.2 deletion syndrome is a common syndrome also known as DiGeorge syndrome and velocardiofacial …
Chromosome 22q11.2 Deletion (DiGeorge Syndrome): Immunologic Features, Diagnosis, and Management.
Biggs SE, Gilchrist B, May KR. Biggs SE, et al. Curr Allergy Asthma Rep. 2023 Apr;23(4):213-222. doi: 10.1007/s11882-023-01071-4. Epub 2023 Mar 10. Curr Allergy Asthma Rep. 2023. PMID: 36897497 Free PMC article. Review.
PURPOSE OF REVIEW: This review focuses on immunologic findings, relationships among immunologic findings and associated conditions of autoimmunity and atopy, and management of immunologic disease in chromosome 22q11.2 deletion syndrome (22q11.2DS, historically known as …
PURPOSE OF REVIEW: This review focuses on immunologic findings, relationships among immunologic findings and associated conditions of autoim …
DiGeorge syndrome: consider the diagnosis.
Altshuler E, Saidi A, Budd J. Altshuler E, et al. BMJ Case Rep. 2022 Feb 2;15(2):e245164. doi: 10.1136/bcr-2021-245164. BMJ Case Rep. 2022. PMID: 35110278 Free PMC article.
DiGeorge syndrome (DGS) is caused by a chromosomal microdeletion at 22q11.2 that results in impaired development of the pharyngeal pouch system. ...
DiGeorge syndrome (DGS) is caused by a chromosomal microdeletion at 22q11.2 that results in impaired development of the pharyn
22q11.2 deletion syndrome.
McDonald-McGinn DM, Sullivan KE, Marino B, Philip N, Swillen A, Vorstman JA, Zackai EH, Emanuel BS, Vermeesch JR, Morrow BE, Scambler PJ, Bassett AS. McDonald-McGinn DM, et al. Nat Rev Dis Primers. 2015 Nov 19;1:15071. doi: 10.1038/nrdp.2015.71. Nat Rev Dis Primers. 2015. PMID: 27189754 Free PMC article. Review.
The first description in the English language of the constellation of findings now known to be due to this chromosomal difference was made in the 1960s in children with DiGeorge syndrome, who presented with the clinical triad of immunodeficiency, hypoparathyroidism …
The first description in the English language of the constellation of findings now known to be due to this chromosomal difference was made i …
Clinical Manifestations of 22q11.2 Deletion Syndrome.
Cirillo A, Lioncino M, Maratea A, Passariello A, Fusco A, Fratta F, Monda E, Caiazza M, Signore G, Esposito A, Baban A, Versacci P, Putotto C, Marino B, Pignata C, Cirillo E, Giardino G, Sarubbi B, Limongelli G, Russo MG. Cirillo A, et al. Heart Fail Clin. 2022 Jan;18(1):155-164. doi: 10.1016/j.hfc.2021.07.009. Epub 2021 Oct 25. Heart Fail Clin. 2022. PMID: 34776076 Review.
DiGeorge syndrome (DGS), also known as "22q11.2 deletion syndrome" (22q11DS) (MIM # 192430 # 188400), is a genetic disorder caused by hemizygous microdeletion of the long arm of chromosome 22. ...
DiGeorge syndrome (DGS), also known as "22q11.2 deletion syndrome" (22q11DS) (MIM # 192430 # 188400), is a genetic diso
DiGeorge syndrome: new insights.
Goldmuntz E. Goldmuntz E. Clin Perinatol. 2005 Dec;32(4):963-78, ix-x. doi: 10.1016/j.clp.2005.09.006. Clin Perinatol. 2005. PMID: 16325672 Review.
Most patients with the clinical features of DiGeorge, velocardiofacial, and conotruncal anomaly face syndromes share a common genetic cause, namely, a deletion of chromosome 22q11, and define the most common deletion syndrome known at this time. The clinical feature …
Most patients with the clinical features of DiGeorge, velocardiofacial, and conotruncal anomaly face syndromes share a common genetic …
LncRNA DiGeorge syndrome critical region gene 5: A crucial regulator in malignant tumors.
Xia H, Huang Z, Liu S, Zhao X, He R, Wang Z, Shi W, Chen W, Li Z, Yu L, Huang P, Kang P, Su Z, Xu Y, Yam JWP, Cui Y. Xia H, et al. Biomed Pharmacother. 2021 Sep;141:111889. doi: 10.1016/j.biopha.2021.111889. Epub 2021 Jul 14. Biomed Pharmacother. 2021. PMID: 34323697 Free article. Review.
Long non-coding RNA (lncRNA), a subgroup of ncRNA with a length of more than 200 nt without protein coding function, has been recognized by the academia for its mediating effects of dysregulated expression on the tumorigenesis and development of a variety of tumors. LncRNA DiG
Long non-coding RNA (lncRNA), a subgroup of ncRNA with a length of more than 200 nt without protein coding function, has been recognized by …
DiGeorge syndrome and pharyngeal apparatus development.
Wurdak H, Ittner LM, Sommer L. Wurdak H, et al. Bioessays. 2006 Nov;28(11):1078-86. doi: 10.1002/bies.20484. Bioessays. 2006. PMID: 17041894 Review.
DiGeorge syndrome is the most frequent microdeletion syndrome in humans, and is characterized by cardiovascular, thymic and parathyroid, and craniofacial anomalies. ...The analysis of engineered mouse mutants developing a phenotype resembling DiGeorge
DiGeorge syndrome is the most frequent microdeletion syndrome in humans, and is characterized by cardiovascular, thymic
Prader-Willi Syndrome Coincident with DiGeorge Syndrome.
Zou XY, Chao YQ, Zeng LH, Zou CC. Zou XY, et al. Indian J Pediatr. 2020 Jun;87(6):471-472. doi: 10.1007/s12098-019-03137-6. Epub 2019 Dec 20. Indian J Pediatr. 2020. PMID: 31863392 No abstract available.
[DiGeorge syndrome].
Hamada H, Terai M. Hamada H, et al. Nihon Rinsho. 2006 Jun 28;Suppl 2:46-8. Nihon Rinsho. 2006. PMID: 16817347 Review. Japanese. No abstract available.
3,563 results