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

Year Number of Results
1980 1
1987 2
1989 1
1990 1
1991 1
1992 2
1993 7
1994 5
1995 7
1996 20
1997 27
1998 27
1999 28
2000 25
2001 43
2002 23
2003 33
2004 35
2005 25
2006 24
2007 38
2008 27
2009 26
2010 23
2011 29
2012 14
2013 25
2014 31
2015 27
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2017 35
2018 23
2019 19
2020 13
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626 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
Velocardiofacial Syndrome.
Bishop BN, Brady R. Bishop BN, et al. 2019 Feb 20. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2020 Jan–. StatPearls. 2020 Jan–. PMID: 30860719 Free Books & Documents. Review.
Angelo Di George , velocardial facial syndrome (otherwise known as Di George syndrome or Chromosome 22q11.2 syndrome) is the most common microdeletion syndrome in humans.  ...Though there are a variety of presentations and phenotypes possible in veloca …
Angelo Di George , velocardial facial syndrome (otherwise known as Di George syndrome or Chromosome 22q11.2 syndrome) i …
Velocardiofacial syndrome.
Pike AC, Super M. Pike AC, et al. Postgrad Med J. 1997 Dec;73(866):771-5. doi: 10.1136/pgmj.73.866.771. Postgrad Med J. 1997. PMID: 9497944 Free PMC article. Review.
Velocardiofacial syndrome is a syndrome of multiple anomalies that include cleft palate, cardiac defects, learning difficulties, speech disorder and characteristic facial features. ...Identification of the syndrome can be difficult as many of the anoma
Velocardiofacial syndrome is a syndrome of multiple anomalies that include cleft palate, cardiac defects, learning diff
Velocardiofacial syndrome.
Gothelf D. Gothelf D. Child Adolesc Psychiatr Clin N Am. 2007 Jul;16(3):677-93. doi: 10.1016/j.chc.2007.03.005. Child Adolesc Psychiatr Clin N Am. 2007. PMID: 17562586 Review.
Velocardiofacial syndrome (VCFS) is the most common known microdeletion in humans. It is also the most common known genetic risk factor for schizophrenia. The aim of this article is to describe the clinical characteristics of the syndrome, with emphasis on th
Velocardiofacial syndrome (VCFS) is the most common known microdeletion in humans. It is also the most common known genetic ri
Velocardiofacial syndrome.
Shprintzen RJ. Shprintzen RJ. Otolaryngol Clin North Am. 2000 Dec;33(6):1217-40, vi. doi: 10.1016/s0030-6665(05)70278-4. Otolaryngol Clin North Am. 2000. PMID: 11449784 Review.
Velocardiofacial syndrome is one of the most common multiple-anomaly syndromes in humans. With its many otolaryngologic manifestations and its almost ubiquitous effects on speech, language, hearing, immune dysfunction, and airway problems, velocardiofacial
Velocardiofacial syndrome is one of the most common multiple-anomaly syndromes in humans. With its many otolaryngologic manife
Clinical presentation and genetic profiles of Chinese patients with velocardiofacial syndrome in a large referral centre.
Wu D, Chen Y, Chen Q, Wang G, Xu X, Peng A, Hao J, He J, Huang L, Dai J. Wu D, et al. J Genet. 2019 Jun;98(2):42. J Genet. 2019. PMID: 31204702 Free article.
Diagnosis and treatment of velocardiofacial syndrome (VCFS) with variable genotypes and phenotypes are considered to be very complicated. ...
Diagnosis and treatment of velocardiofacial syndrome (VCFS) with variable genotypes and phenotypes are considered to be very c …
Speech Therapy in Velocardiofacial Syndrome After Palatopharyngeal Pharyngoplasty.
Jiang L, Yang Y, Liu Q. Jiang L, et al. J Craniofac Surg. 2018 Oct;29(7):1709-1712. doi: 10.1097/SCS.0000000000004629. J Craniofac Surg. 2018. PMID: 29863556
Velocardiofacial syndrome (VCFs) is a rare congenital disease with an incidence of 1:4000 to 1:6000. Previous studies have found that the abnormality is associated with 22qDS. As reported at the international VCFs conference held in 2006, >180 phenotypes have bee
Velocardiofacial syndrome (VCFs) is a rare congenital disease with an incidence of 1:4000 to 1:6000. Previous studies have fou
DiGeorge Syndrome.
Lackey AE, Muzio MR. Lackey AE, et al. 2020 Jun 30. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2020 Jan–. StatPearls. 2020 Jan–. PMID: 31747205 Free Books & Documents. Review.
DiGeorge Syndrome (DGS) is a combination of signs and symptoms caused by defects in the development of structures derived from the pharyngeal arches during embryogenesis. ...DGS is one of several syndromes that has historically grouped under a bigger umbrella called 22q11 …
DiGeorge Syndrome (DGS) is a combination of signs and symptoms caused by defects in the development of structures derived from the ph …
22q11.2 Deletion Syndrome.
McDonald-McGinn DM, Hain HS, Emanuel BS, Zackai EH. McDonald-McGinn DM, et al. 1999 Sep 23 [updated 2020 Feb 27]. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2020. GeneReviews®. 1993–2020. PMID: 20301696 Free Books & Documents. Review.
CLINICAL CHARACTERISTICS: Individuals with 22q11.2 deletion syndrome (22q11.2DS) can present with a wide range of features that are highly variable, even within families. ...GENETIC COUNSELING: 22q11.2DS is an autosomal dominant contiguous gene deletion syndrome. In …
CLINICAL CHARACTERISTICS: Individuals with 22q11.2 deletion syndrome (22q11.2DS) can present with a wide range of features that are h …
Bernard-Soulier syndrome associated with 22q11.2 deletion and clinical features of DiGeorge/velocardiofacial syndrome.
Souto Filho JTD, Ribeiro HAA, Fassbender IPB, Ribeiro JMMC, Ferreira Júnior WDS, Figueiredo LCS. Souto Filho JTD, et al. Blood Coagul Fibrinolysis. 2019 Dec;30(8):423-425. doi: 10.1097/MBC.0000000000000849. Blood Coagul Fibrinolysis. 2019. PMID: 31738289
: Bernard-Soulier syndrome (BSS) is a rare autosomal recessive bleeding disorder caused by a defective function of glycoprotein (GP) Ib-V-IX complex. ...We report a case of a girl with BSS associated with clinical features of 22q11.2 deletion syndrome (22q11.2DS) wi …
: Bernard-Soulier syndrome (BSS) is a rare autosomal recessive bleeding disorder caused by a defective function of glycoprotein (GP) …
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