174 related articles for article (PubMed ID: 8194832)
1. Deciphering the molecular genetics of congenital heart disease.
Bouvagnet P; Sauer U; Debrus S; Genz T; Alonso S; Berger G; De Meeus A; Bühlmeier K; Demaille J
Herz; 1994 Apr; 19(2):119-25. PubMed ID: 8194832
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Genetic background of congenital conotruncal heart defects--a study of 45 families.
Kwiatkowska J; Wierzba J; Aleszewicz-Baranowska J; Ereciński J
Kardiol Pol; 2007 Jan; 65(1):32-7; discussion 38-9. PubMed ID: 17295158
[TBL] [Abstract][Full Text] [Related]
4. Congenital cardiac defects with 22q11 deletion.
Giray O; Ulgenalp A; Bora E; Sağin Saylam G; Unal N; Meşe T; Hüdaoğlu S; Erçal D
Turk J Pediatr; 2003; 45(3):217-20. PubMed ID: 14696799
[TBL] [Abstract][Full Text] [Related]
5. [Autosomal dominant Mendelian midline complex. Secundum atrial septal defect associated with cardiac and facial-thoracic defects. A familial case].
Stéphan E; Ashoush R; Mégarbané A; Kassab R; Salem N; Loiselet J; Bouvagnet P
Arch Mal Coeur Vaiss; 2000 May; 93(5):641-7. PubMed ID: 10858865
[TBL] [Abstract][Full Text] [Related]
6. Role of the vascular endothelial growth factor isoforms in retinal angiogenesis and DiGeorge syndrome.
Stalmans I
Verh K Acad Geneeskd Belg; 2005; 67(4):229-76. PubMed ID: 16334858
[TBL] [Abstract][Full Text] [Related]
7. [Congenital cardiopathies and syndromes in adults].
Calderón Colmenero J
Arch Cardiol Mex; 2002; 72 Suppl 1():S31-4. PubMed ID: 12001867
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. 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]
10. 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]
11. Conotruncal heart defects: impact of genetic syndromes on immediate operative mortality.
Anaclerio S; Di Ciommo V; Michielon G; Digilio MC; Formigari R; Picchio FM; Gargiulo G; Di Donato R; De Ioris MA; Marino B
Ital Heart J; 2004 Aug; 5(8):624-8. PubMed ID: 15554034
[TBL] [Abstract][Full Text] [Related]
12. Chromosome 22q11 deletion syndrome: the first three cases reported in Thailand.
Ruangdaraganon N; Tocharoentanaphol C; Khowsathit P; Sombuntham T; Pongpanich B
J Med Assoc Thai; 1999 Nov; 82 Suppl 1():S179-85. PubMed ID: 10730540
[TBL] [Abstract][Full Text] [Related]
13. [Epidemiology and genetics of congenital heart diseases and cardiomyopathies in children].
Bonnet D
Rev Prat; 2006 Mar; 56(6):599-604. PubMed ID: 16705916
[TBL] [Abstract][Full Text] [Related]
14. 22q11.2 deletion syndrome in Singapore (2000-2003): a case for active ascertainment.
Tan KB; Chew SK; Yeo GS
Singapore Med J; 2008 Apr; 49(4):286-9. PubMed ID: 18418519
[TBL] [Abstract][Full Text] [Related]
15. The genetics of congenital heart disease: a review of recent developments.
Weismann CG; Gelb BD
Curr Opin Cardiol; 2007 May; 22(3):200-6. PubMed ID: 17413276
[TBL] [Abstract][Full Text] [Related]
16. Congenital heart defects--chromosomal anomalies, syndromes and extracardiac malformations.
Meberg A; Hals J; Thaulow E
Acta Paediatr; 2007 Aug; 96(8):1142-5. PubMed ID: 17590185
[TBL] [Abstract][Full Text] [Related]
17. Kabuki syndrome is not caused by a microdeletion in the DiGeorge/velocardiofacial chromosomal region within 22q 11.2.
Li M; Zackai EH; Niikawa N; Kaplan P; Driscoll DA
Am J Med Genet; 1996 Oct; 65(2):101-3. PubMed ID: 8911598
[TBL] [Abstract][Full Text] [Related]
18. Lack of evidence for connexin 43 gene mutations in human autosomal recessive lateralization defects.
Debrus S; Tuffery S; Matsuoka R; Galal O; Sarda P; Sauer U; Bozio A; Tanman B; Toutain A; Claustres M; Le Paslier D; Bouvagnet P
J Mol Cell Cardiol; 1997 May; 29(5):1423-31. PubMed ID: 9201627
[TBL] [Abstract][Full Text] [Related]
19. Genetics of congenital heart diseases in syndromic and non-syndromic patients: new advances and clinical implications.
Piacentini G; Digilio MC; Sarkozy A; Placidi S; Dallapiccola B; Marino B
J Cardiovasc Med (Hagerstown); 2007 Jan; 8(1):7-11. PubMed ID: 17255809
[TBL] [Abstract][Full Text] [Related]
20. [Molecular aspects of congenital heart diseases].
Bajolle F; Zaffran S; Bonnet D
Arch Mal Coeur Vaiss; 2007 May; 100(5):484-9. PubMed ID: 17646780
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]