663 related articles for article (PubMed ID: 16325672)
1. DiGeorge syndrome: new insights.
Goldmuntz E
Clin Perinatol; 2005 Dec; 32(4):963-78, ix-x. PubMed ID: 16325672
[TBL] [Abstract][Full Text] [Related]
2. Cardiac defects and results of cardiac surgery in 22q11.2 deletion syndrome.
Carotti A; Digilio MC; Piacentini G; Saffirio C; Di Donato RM; Marino B
Dev Disabil Res Rev; 2008; 14(1):35-42. PubMed ID: 18636635
[TBL] [Abstract][Full Text] [Related]
3. Congenital heart defects in patients with DiGeorge/velocardiofacial syndrome and del22q11.
Marino B; Digilio MC; Toscano A; Giannotti A; Dallapiccola B
Genet Couns; 1999; 10(1):25-33. PubMed ID: 10191426
[TBL] [Abstract][Full Text] [Related]
4. CATCH 22 syndrome: report of 7 infants with follow-up data and review of the recent advancements in the genetic knowledge of the locus 22q11.
Sergi C; Serpi M; Müller-Navia J; Schnabel PA; Hagl S; Otto HF; Ulmer HE
Pathologica; 1999 Jun; 91(3):166-72. PubMed ID: 10536461
[TBL] [Abstract][Full Text] [Related]
5. Tetralogy of Fallot with pulmonary atresia associated with chromosome 22q11 deletion.
Momma K; Kondo C; Matsuoka R
J Am Coll Cardiol; 1996 Jan; 27(1):198-202. PubMed ID: 8522695
[TBL] [Abstract][Full Text] [Related]
6. Confirmation that the conotruncal anomaly face syndrome is associated with a deletion within 22q11.2.
Matsuoka R; Takao A; Kimura M; Imamura S; Kondo C; Joh-o K; Ikeda K; Nishibatake M; Ando M; Momma K
Am J Med Genet; 1994 Nov; 53(3):285-9. PubMed ID: 7856665
[TBL] [Abstract][Full Text] [Related]
7. The Philadelphia story: the 22q11.2 deletion: report on 250 patients.
McDonald-McGinn DM; Kirschner R; Goldmuntz E; Sullivan K; Eicher P; Gerdes M; Moss E; Solot C; Wang P; Jacobs I; Handler S; Knightly C; Heher K; Wilson M; Ming JE; Grace K; Driscoll D; Pasquariello P; Randall P; Larossa D; Emanuel BS; Zackai EH
Genet Couns; 1999; 10(1):11-24. PubMed ID: 10191425
[TBL] [Abstract][Full Text] [Related]
8. 22q11.2 deletion syndrome and congenital heart disease.
Goldmuntz E
Am J Med Genet C Semin Med Genet; 2020 Mar; 184(1):64-72. PubMed ID: 32049433
[TBL] [Abstract][Full Text] [Related]
9. The DiGeorge anomaly (CATCH 22, DiGeorge/velocardiofacial syndrome).
Hong R
Semin Hematol; 1998 Oct; 35(4):282-90. PubMed ID: 9801257
[TBL] [Abstract][Full Text] [Related]
10. [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]
11. [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]
12. Chromosome 22q11 deletions in patients with selected outflow tract malformations.
Frohn-Mulder IM; Wesby Swaay E; Bouwhuis C; Van Hemel JO; Gerritsma E; Niermeyer MF; Hess J
Genet Couns; 1999; 10(1):35-41. PubMed ID: 10191427
[TBL] [Abstract][Full Text] [Related]
13. Cardiovascular anomalies associated with chromosome 22q11.2 deletion syndrome.
Momma K
Am J Cardiol; 2010 Jun; 105(11):1617-24. PubMed ID: 20494672
[TBL] [Abstract][Full Text] [Related]
14. [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]
15. 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]
16. Frequency of 22q11 deletions in patients with conotruncal defects.
Goldmuntz E; Clark BJ; Mitchell LE; Jawad AF; Cuneo BF; Reed L; McDonald-McGinn D; Chien P; Feuer J; Zackai EH; Emanuel BS; Driscoll DA
J Am Coll Cardiol; 1998 Aug; 32(2):492-8. PubMed ID: 9708481
[TBL] [Abstract][Full Text] [Related]
17. [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]
18. DiGeorge anomaly in the absence of chromosome 22q11.2 deletion.
Rope AF; Cragun DL; Saal HM; Hopkin RJ
J Pediatr; 2009 Oct; 155(4):560-5. PubMed ID: 19595366
[TBL] [Abstract][Full Text] [Related]
19. Neural tube defects and deletions of 22q11.
Nickel RE; Magenis RE
Am J Med Genet; 1996 Dec; 66(1):25-7. PubMed ID: 8957506
[TBL] [Abstract][Full Text] [Related]
20. Microdeletion 22q11 and oesophageal atresia.
Digilio MC; Marino B; Bagolan P; Giannotti A; Dallapiccola B
J Med Genet; 1999 Feb; 36(2):137-9. PubMed ID: 10051013
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
