230 related articles for article (PubMed ID: 17255809)
1. 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]
2. Heritable syndromes with skeletal abnormalities and congenital heart disease.
Martin EC
N Y State J Med; 1977 May; 77(6):944-50. PubMed ID: 140338
[No Abstract] [Full Text] [Related]
3. [Genetic study of children with congenital heart defects].
Fäller K; Szollár J
Orv Hetil; 1984 Aug; 125(34):2071-5. PubMed ID: 6237297
[No Abstract] [Full Text] [Related]
4. Atrioventricular canal defect without Down syndrome: a heterogeneous malformation.
Digilio MC; Marino B; Toscano A; Giannotti A; Dallapiccola B
Am J Med Genet; 1999 Jul; 85(2):140-6. PubMed ID: 10406667
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. 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]
7. An unusual cardiac defect in a patient with clinical features overlapping between cardiofaciocutaneous and Noonan syndromes.
DeSena HC; Niyazov DM; Parrino PE; Lucas VW; Shah SB; Moodie DS
Congenit Heart Dis; 2010; 5(1):70-5. PubMed ID: 20136862
[TBL] [Abstract][Full Text] [Related]
8. Congenital heart disease and genetic syndromes: new insights into molecular mechanisms.
Calcagni G; Unolt M; Digilio MC; Baban A; Versacci P; Tartaglia M; Baldini A; Marino B
Expert Rev Mol Diagn; 2017 Sep; 17(9):861-870. PubMed ID: 28745539
[TBL] [Abstract][Full Text] [Related]
9. [The Holt-Oram syndrome. Entelechy or clinical entity? A mild form of familial presentation].
Palma Nieto JC; Herráez García J; Sciaccaluga Morelli C; Briones García JL
Rev Esp Cardiol; 1993 Jun; 46(6):385-8. PubMed ID: 8316706
[TBL] [Abstract][Full Text] [Related]
10. Population-based study of congenital heart defects in Down syndrome.
Freeman SB; Taft LF; Dooley KJ; Allran K; Sherman SL; Hassold TJ; Khoury MJ; Saker DM
Am J Med Genet; 1998 Nov; 80(3):213-7. PubMed ID: 9843040
[TBL] [Abstract][Full Text] [Related]
11. The Noonan-CFC controversy.
Neri G; Zollino M; Reynolds JF
Am J Med Genet; 1991 Jun; 39(3):367-70. PubMed ID: 1867292
[TBL] [Abstract][Full Text] [Related]
12. Non-cardiac malformations in individuals with outflow tract defects of the heart: the Baltimore-Washington Infant Study (1981-1989).
Lurie IW; Kappetein AP; Loffredo CA; Ferencz C
Am J Med Genet; 1995 Oct; 59(1):76-84. PubMed ID: 8849016
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Genetic syndromes and congenital heart defects: how is surgical management affected?
Formigari R; Michielon G; Digilio MC; Piacentini G; Carotti A; Giardini A; Di Donato RM; Marino B
Eur J Cardiothorac Surg; 2009 Apr; 35(4):606-14. PubMed ID: 19091590
[TBL] [Abstract][Full Text] [Related]
15. The spectrum of cardiac anomalies in Noonan syndrome as a result of mutations in the PTPN11 gene.
Sznajer Y; Keren B; Baumann C; Pereira S; Alberti C; Elion J; Cavé H; Verloes A
Pediatrics; 2007 Jun; 119(6):e1325-31. PubMed ID: 17515436
[TBL] [Abstract][Full Text] [Related]
16. Ellis van Creveld syndrome (chondroectodermal dysplasia, MIM 22550) in three siblings from a non-consanguineous mating.
George E; DeSilva S; Lieber E; Raziuddin K; Gudavalli M
J Perinat Med; 2000; 28(6):425-7. PubMed ID: 11155425
[TBL] [Abstract][Full Text] [Related]
17. Impact of DEL22q11, trisomy 21, and other genetic syndromes on surgical outcome of conotruncal heart defects.
Michielon G; Marino B; Oricchio G; Digilio MC; Iorio F; Filippelli S; Placidi S; Di Donato RM
J Thorac Cardiovasc Surg; 2009 Sep; 138(3):565-570.e2. PubMed ID: 19698836
[TBL] [Abstract][Full Text] [Related]
18. What Is New in Genetics of Congenital Heart Defects?
Digilio MC; Marino B
Front Pediatr; 2016; 4():120. PubMed ID: 27990414
[TBL] [Abstract][Full Text] [Related]
19. A Turkish family with Ellis-van Creveld syndrome in six siblings; linkage analysis on 4p16 region (D4S3360-D4S2366).
Cağdaş DN; Parlar AI; Pac A; Tutun U; Balci S
Genet Couns; 2008; 19(4):387-95. PubMed ID: 19239082
[TBL] [Abstract][Full Text] [Related]
20. The association of split hand foot malformation (SHFM) and congenital heart defects.
Elliott AM; Evans JA
Birth Defects Res A Clin Mol Teratol; 2008 Jun; 82(6):425-34. PubMed ID: 18383509
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]