347 related articles for article (PubMed ID: 14696799)
21. Screening of patients at risk for 22q11 deletion.
Barisić I; Morozin Pohovski L; Petković I; Cvetko Z; Stipancić G; Bagatin M
Coll Antropol; 2008 Mar; 32(1):165-9. PubMed ID: 18494202
[TBL] [Abstract][Full Text] [Related]
22. Prenatal diagnosis of 22q11 microdeletion.
Levy-Mozziconacci A; Piquet C; Heurtevin PC; Philip N
Prenat Diagn; 1997 Nov; 17(11):1033-7. PubMed ID: 9399351
[TBL] [Abstract][Full Text] [Related]
23. Allelic variations at the haploid TBX1 locus do not influence the cardiac phenotype in cases of 22q11 microdeletion.
Voelckel MA; Girardot L; Giusiano B; Levy N; Philip N
Ann Genet; 2004; 47(3):235-40. PubMed ID: 15337468
[TBL] [Abstract][Full Text] [Related]
24. Atypical 22q11 microdeletions in Iranian patients with congenital conotruncal cardiac defects.
Pouranvari S; Noruzinia M; Ghafari RS; Zeinaloo AA; Kaviani S
Saudi Med J; 2008 Oct; 29(10):1514-6. PubMed ID: 18946587
[No Abstract] [Full Text] [Related]
25. 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]
26. [Risk of missed diagnosis of 22q11.2 deletion in a fetal cardiac conotruncal malformation when another chromosomal abnormality is detected].
Picone O; Brisset S; Senat MV; Maurin ML; Frydman R; Tachdjian G
J Gynecol Obstet Biol Reprod (Paris); 2008 May; 37(3):299-301. PubMed ID: 18160230
[TBL] [Abstract][Full Text] [Related]
27. [Chromosome 22 (22q.11.2) deletion. Etiology of conotruncal heart abnormalities].
Buendía Hernández A; Calderón-Colmenero J; Aizpuru E; Attie CL; Zabal C; Patiño E; Miranda I; Juanico A; Attie F
Arch Inst Cardiol Mex; 2000; 70(2):148-53. PubMed ID: 10932799
[TBL] [Abstract][Full Text] [Related]
28. Cardiovascular anomalies in patients with chromosome 22q11.2 deletion: a Korean multicenter study.
Park IS; Ko JK; Kim YH; Yoo HW; Seo EJ; Choi JY; Gil HY; Kim SJ
Int J Cardiol; 2007 Jan; 114(2):230-5. PubMed ID: 16824627
[TBL] [Abstract][Full Text] [Related]
29. [22q11 deletion in conotruncal anomalies].
Kádár K
Orv Hetil; 2005 Feb; 146(8):363-6. PubMed ID: 15803887
[TBL] [Abstract][Full Text] [Related]
30. [A study on the occurrence of the deletion 22q11.2 in patients affected with a psychiatric disease].
Pawłowska B; Tomankiewicz-Zawadzka A; Ilnicka A; Bogdanowicz J; Wciórka J; Szafrański T; Woźniak P; Meder J; Szaniawska-Bartnicka A; Zdzienicka E; Szirkowiec W; Zaremba J
Psychiatr Pol; 2007; 41(2):251-60. PubMed ID: 17598434
[TBL] [Abstract][Full Text] [Related]
31. Dysplastic changes in the peripheral blood of children with microdeletion 22q11.2.
Ozbek N; Derbent M; Olcay L; Yilmaz Z; Tokel K
Am J Hematol; 2004 Oct; 77(2):126-31. PubMed ID: 15389824
[TBL] [Abstract][Full Text] [Related]
32. Prevalence of the microdeletion 22q11 in newborn infants with congenital conotruncal cardiac anomalies.
Iserin L; de Lonlay P; Viot G; Sidi D; Kachaner J; Munnich A; Lyonnet S; Vekemans M; Bonnet D
Eur J Pediatr; 1998 Nov; 157(11):881-4. PubMed ID: 9835429
[TBL] [Abstract][Full Text] [Related]
33. Prenatal diagnosis of a 22q11 deletion in a second-trimester fetus with conotruncal anomaly, absent thymus and meningomyelocele: Kousseff syndrome.
Canda MT; Demir N; Bal FU; Doganay L; Sezer O
J Obstet Gynaecol Res; 2012 Apr; 38(4):737-40. PubMed ID: 22380655
[TBL] [Abstract][Full Text] [Related]
34. Detection of chromosomal abnormalities and the 22q11 microdeletion in fetuses with congenital heart defects.
Lv W; Wang S
Mol Med Rep; 2014 Nov; 10(5):2465-70. PubMed ID: 25215544
[TBL] [Abstract][Full Text] [Related]
35. PCR assay for screening patients at risk for 22q11.2 deletion.
Driscoll DA; Emanuel BS; Mitchell LE; Budarf ML
Genet Test; 1997; 1(2):109-13. PubMed ID: 10464634
[TBL] [Abstract][Full Text] [Related]
36. Chromosomal abnormalities among children born with conotruncal cardiac defects.
Lammer EJ; Chak JS; Iovannisci DM; Schultz K; Osoegawa K; Yang W; Carmichael SL; Shaw GM
Birth Defects Res A Clin Mol Teratol; 2009 Jan; 85(1):30-5. PubMed ID: 19067405
[TBL] [Abstract][Full Text] [Related]
37. [Neonatal hypocalcaemic dilated myocardiopathy due to a 22q11 microdeletion].
Goulet M; Rio M; Jacquette A; Ladouceur M; Bonnet D
Arch Mal Coeur Vaiss; 2006 May; 99(5):520-2. PubMed ID: 16802747
[TBL] [Abstract][Full Text] [Related]
38. Detection of a 22q11.2 deletion in cardiac patients suggests a risk for velopharyngeal incompetence.
McDonald-McGinn DM; Driscoll DA; Emanuel BS; Goldmuntz E; Clark BJ; Solot C; Cohen M; Schultz P; LaRossa D; Randall P; Zackai EH
Pediatrics; 1997 May; 99(5):E9. PubMed ID: 9113966
[TBL] [Abstract][Full Text] [Related]
39. Conotruncal anomaly face syndrome is associated with a deletion within chromosome 22q11.
Burn J; Takao A; Wilson D; Cross I; Momma K; Wadey R; Scambler P; Goodship J
J Med Genet; 1993 Oct; 30(10):822-4. PubMed ID: 8230157
[TBL] [Abstract][Full Text] [Related]
40. Associated anomalies in asymmetric crying facies and 22q11 deletion.
Akcakus M; Ozkul Y; Gunes T; Kurtoglu S; Cetin N; Kisaarslan AP; Dundar M
Genet Couns; 2003; 14(3):325-30. PubMed ID: 14577677
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]