167 related articles for article (PubMed ID: 21846625)
1. Chromosome 22q11.2 microdeletion syndrome.
Molesky MG
Neonatal Netw; 2011; 30(5):304-11. PubMed ID: 21846625
[TBL] [Abstract][Full Text] [Related]
2. [22q11.2 chromosome deletion and velo-cardio-facial syndrome in a patient with tetralogy of Fallot].
Morava E; Masszi G; Czakó M; Tóth G; Melegh B; Kosztolányi G
Orv Hetil; 2000 Aug; 141(34):1873-5. PubMed ID: 11006712
[TBL] [Abstract][Full Text] [Related]
3. [Improvement of genetic diagnostic strategy in velo-cardio-facial syndrome].
Pânzaru M; Rusu C; Voloşciuc M; Braha E; Butnariu L; Ivanov I; Grămescu M; Popescu R; Caba L; Sireteanu A; Macovei M; Covic M; Gorduza EV
Rev Med Chir Soc Med Nat Iasi; 2011; 115(3):756-61. PubMed ID: 22046783
[TBL] [Abstract][Full Text] [Related]
4. [Relationship between 22q11 microdeletion syndrome and congenital heart disease].
Qin YF; Xie CH; Yang JB; Wu DW; Shao J; Zhao ZY
Zhonghua Xin Xue Guan Bing Za Zhi; 2011 Jul; 39(7):631-5. PubMed ID: 22088244
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Laryngeal atresia type III (glottic web) with 22q11.2 microdeletion: report of three patients.
Fokstuen S; Bottani A; Medeiros PF; Antonarakis SE; Stoll C; Schinzel A
Am J Med Genet; 1997 May; 70(2):130-3. PubMed ID: 9128930
[TBL] [Abstract][Full Text] [Related]
7. Classical Noonan syndrome is not associated with deletions of 22q11.
Robin NH; Sellinger B; McDonald-McGinn D; Zackai EH; Emanuel BS; Driscoll DA
Am J Med Genet; 1995 Mar; 56(1):94-6. PubMed ID: 7747795
[TBL] [Abstract][Full Text] [Related]
8. [Clinical heterogeneity of the chromosome 22q11 microdeletion syndrome].
Muñoz S; Garay F; Flores I; Heusser F; Talesnik E; Aracena M; Mellado C; Méndez C; Arnaiz P; Repetto G
Rev Med Chil; 2001 May; 129(5):515-21. PubMed ID: 11464533
[TBL] [Abstract][Full Text] [Related]
9. Velo-cardio-facial syndrome: guidelines for diagnosis, treatment and follow-up of ent manifestations.
Vantrappen G; Rommel N; Swillen A; Cremers CW; Fryns JP; Devriendt K
Acta Otorhinolaryngol Belg; 2003; 57(2):101-6. PubMed ID: 12836465
[TBL] [Abstract][Full Text] [Related]
10. Hypocalcemia and chromosome 22q11 microdeletion.
Garabédian M
Genet Couns; 1999; 10(4):389-94. PubMed ID: 10631928
[TBL] [Abstract][Full Text] [Related]
11. [Syndromes 3. Velo-cardio-facial (VCF/Shprintzen) syndrome].
Beemer FA
Ned Tijdschr Tandheelkd; 1998 Aug; 105(8):287-8. PubMed ID: 11928434
[TBL] [Abstract][Full Text] [Related]
12. Velo-cardio-facial syndrome and DiGeorge sequence with meningomyelocele and deletions of the 22q11 region.
Nickel RE; Pillers DA; Merkens M; Magenis RE; Driscoll DA; Emanuel BS; Zonana J
Am J Med Genet; 1994 Oct; 52(4):445-9. PubMed ID: 7747757
[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. Immunologic features of chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome).
Jawad AF; McDonald-Mcginn DM; Zackai E; Sullivan KE
J Pediatr; 2001 Nov; 139(5):715-23. PubMed ID: 11713452
[TBL] [Abstract][Full Text] [Related]
15. Confirmation that the velo-cardio-facial syndrome is associated with haplo-insufficiency of genes at chromosome 22q11.
Kelly D; Goldberg R; Wilson D; Lindsay E; Carey A; Goodship J; Burn J; Cross I; Shprintzen RJ; Scambler PJ
Am J Med Genet; 1993 Feb; 45(3):308-12. PubMed ID: 8434616
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Velo-cardio-facial syndrome: frequency and extent of 22q11 deletions.
Lindsay EA; Goldberg R; Jurecic V; Morrow B; Carlson C; Kucherlapati RS; Shprintzen RJ; Baldini A
Am J Med Genet; 1995 Jul; 57(3):514-22. PubMed ID: 7677167
[TBL] [Abstract][Full Text] [Related]
18. Detection of 22q11.2 deletion among 139 patients with Di George/Velocardiofacial syndrome features.
Kitsiou-Tzeli S; Kolialexi A; Fryssira H; Galla-Voumvouraki A; Salavoura K; Kanariou M; Tsangaris GT; Kanavakis E; Mavrou A
In Vivo; 2004; 18(5):603-8. PubMed ID: 15523900
[TBL] [Abstract][Full Text] [Related]
19. [Cerebral polymicrogyria and 22q11 deletion syndrome].
Arriola-Pereda G; Verdú-Pérez A; de Castro-De Castro P
Rev Neurol; 2009 Feb 16-28; 48(4):188-90. PubMed ID: 19226486
[TBL] [Abstract][Full Text] [Related]
20. Microdeletion of 22q11 (CATCH 22) in children with conotruncal heart defect and extracardiac malformations.
Alikaşifoğlu M; Malkoç N; Ceviz N; Ozme S; Uludoğan S; Tunçbilek E
Turk J Pediatr; 2000; 42(3):215-8. PubMed ID: 11105620
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]