172 related articles for article (PubMed ID: 34103968)
1. The Oral Health of Patients with DiGeorge Syndrome (22q11) Microdeletion: A Case Report.
Candelo E; Estrada-Mesa MA; Jaramillo A; Martinez-Cajas CH; Osorio JC; Pachajoa H
Appl Clin Genet; 2021; 14():267-277. PubMed ID: 34103968
[TBL] [Abstract][Full Text] [Related]
2. Oral manifestations in 22q11 deletion syndrome.
Klingberg G; Oskarsdóttir S; Johannesson EL; Norén JG
Int J Paediatr Dent; 2002 Jan; 12(1):14-23. PubMed ID: 11853243
[TBL] [Abstract][Full Text] [Related]
3. Dental management of a patient with 22q11.2 deletion syndrome (22q11.2DS).
AlQarni MA; Alharbi A; Merdad L
BMJ Case Rep; 2018 Sep; 2018():. PubMed ID: 30232069
[TBL] [Abstract][Full Text] [Related]
4. Microdeletion and microduplication 22q11.2 screening in 295 patients with clinical features of DiGeorge/Velocardiofacial syndrome.
Brunet A; Gabau E; Perich RM; Valdesoiro L; Brun C; Caballín MR; Guitart M
Am J Med Genet A; 2006 Nov; 140(22):2426-32. PubMed ID: 17041934
[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. Dental developmental disturbances in 50 individuals with the 22q11.2 deletion syndrome; relation to medical conditions?
Nordgarden H; Lima K; Skogedal N; Følling I; Storhaug K; Abrahamsen TG
Acta Odontol Scand; 2012 May; 70(3):194-201. PubMed ID: 22070626
[TBL] [Abstract][Full Text] [Related]
7. DiGeorge syndrome with microdeletion of chromosome 22q11.2: report of one case.
Wang JL; Chen SJ; Chung MY; Niu DM; Lin CY; Hwang BT; Lu JH
Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi; 1997; 38(5):385-9. PubMed ID: 9401184
[TBL] [Abstract][Full Text] [Related]
8. [DiGeorge syndrome. Velocardiofacial syndrome/chromosome 22q11 deletion syndrome].
Hoffmann MH; Vadstrup S
Ugeskr Laeger; 2000 May; 162(19):2736-9. PubMed ID: 10827540
[TBL] [Abstract][Full Text] [Related]
9. Malocclusions and craniofacial anomalies in a child with velo-cardio-facial syndrome.
Matthews-Brzozowska T; Baranowska J; Rogiński P; Obersztyn E; Cudziło D
Dev Period Med; 2015; 19(4):490-5. PubMed ID: 26982759
[TBL] [Abstract][Full Text] [Related]
10. DiGeorge/velocardiofacial syndrome: FISH studies of chromosomes 22q11 and 10p14, and clinical reports on the proximal 22q11 deletion.
Bartsch O; Nemecková M; Kocárek E; Wagner A; Puchmajerová A; Poppe M; Ounap K; Goetz P
Am J Med Genet A; 2003 Feb; 117A(1):1-5. PubMed ID: 12548732
[TBL] [Abstract][Full Text] [Related]
11. [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]
12. Dental aspects in patients with DiGeorge syndrome.
Toka O; Karl M; Dittrich S; Holst S; Holst A
Quintessence Int; 2010; 41(7):551-6. PubMed ID: 20614041
[TBL] [Abstract][Full Text] [Related]
13. [Growth hormone deficiency associated with 22q11.2 deletion: a case report].
Bizzocchi A; Genoni G; Petri A; Prodam F; Negro M; Bellone S; Bona G
Minerva Pediatr; 2011 Dec; 63(6):527-31. PubMed ID: 22075807
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Endocrine manifestations of chromosome 22q11.2 microdeletion syndrome.
Choi JH; Shin YL; Kim GH; Seo EJ; Kim Y; Park IS; Yoo HW
Horm Res; 2005; 63(6):294-9. PubMed ID: 15995343
[TBL] [Abstract][Full Text] [Related]
16. A Comprehensive Craniofacial Study of 22q11.2 Deletion Syndrome.
Lewyllie A; Roosenboom J; Indencleef K; Claes P; Swillen A; Devriendt K; Carels C; Cadenas De Llano-Pérula M; Willems G; Hens G; Verdonck A
J Dent Res; 2017 Nov; 96(12):1386-1391. PubMed ID: 28732176
[TBL] [Abstract][Full Text] [Related]
17. [Congenital cardiovascular malformations and chromosome microdeletions in 22q11.2].
Trost D; Engels H; Bauriedel G; Wiebe W; Schwanitz G
Dtsch Med Wochenschr; 1999 Jan; 124(1-2):3-7. PubMed ID: 9951451
[TBL] [Abstract][Full Text] [Related]
18. Frequency of 22q11.2 microdeletion in children with congenital heart defects in western poland.
Wozniak A; Wolnik-Brzozowska D; Wisniewska M; Glazar R; Materna-Kiryluk A; Moszura T; Badura-Stronka M; Skolozdrzy J; Krawczynski MR; Zeyland J; Bobkowski W; Slomski R; Latos-Bielenska A; Siwinska A
BMC Pediatr; 2010 Dec; 10():88. PubMed ID: 21134246
[TBL] [Abstract][Full Text] [Related]
19. Medical and dental characteristics of children with chromosome 22q11.2 deletion syndrome at the Royal Children's Hospital, Melbourne.
Wong DH; Rajan S; Hallett KB; Manton DJ
Int J Paediatr Dent; 2021 Nov; 31(6):682-690. PubMed ID: 33222329
[TBL] [Abstract][Full Text] [Related]
20. Noncardiac DiGeorge syndrome diagnosed with multiplex ligation-dependent probe amplification: A case report.
Fu CH; Leung C; Kao CH; Yeh SJ
J Formos Med Assoc; 2015 Aug; 114(8):769-73. PubMed ID: 26254176
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
