-
1
-
-
0034184113
-
Congenital heart malformations: Prevalence, severity, survival, and quality of life
-
Samanek M. Congenital heart malformations: prevalence, severity, survival, and quality of life. Cardiol Young 2000;10:179-85.
-
(2000)
Cardiol Young
, vol.10
, pp. 179-185
-
-
Samanek, M.1
-
2
-
-
0033596673
-
Detection of transposition of the great arteries in fetuses reduces neonatal morbidity and mortality
-
Bonnet D, Coltri A, Butera G, et al. Detection of transposition of the great arteries in fetuses reduces neonatal morbidity and mortality. Circulation 1999:99:916-8.
-
(1999)
Circulation
, vol.99
, pp. 916-918
-
-
Bonnet, D.1
Coltri, A.2
Butera, G.3
-
3
-
-
0033611737
-
Syndromes and malformations associated with congenital heart disease in a population-based study
-
Grech V, Gatt M. Syndromes and malformations associated with congenital heart disease in a population-based study, Int J Cardiol 1999;68:151-6.
-
(1999)
Int J Cardiol
, vol.68
, pp. 151-156
-
-
Grech, V.1
Gatt, M.2
-
4
-
-
0024476864
-
Congenital cardiovascular malformations associated with chromosome abnormalities: An epidemiologic study
-
Ferencz C, Neill CA, Boughman JA, Rubin JD, Brenner JI, Perry LW. Congenital cardiovascular malformations associated with chromosome abnormalities: an epidemiologic study. J Pediatr 1989;114:79-86.
-
(1989)
J Pediatr
, vol.114
, pp. 79-86
-
-
Ferencz, C.1
Neill, C.A.2
Boughman, J.A.3
Rubin, J.D.4
Brenner, J.I.5
Perry, L.W.6
-
5
-
-
0035651517
-
Cardiovascular anomalies in patients diagnosed with a chromosome 22q11 deletion beyond 6 months of age
-
McElhinney DB, McDonald-McGinn D, Zackai EH, Goldmuntz E. Cardiovascular anomalies in patients diagnosed with a chromosome 22q11 deletion beyond 6 months of age. Pediatrics 2001;108:E104.
-
(2001)
Pediatrics
, vol.108
-
-
McElhinney, D.B.1
McDonald-McGinn, D.2
Zackai, E.H.3
Goldmuntz, E.4
-
6
-
-
0028321388
-
Complete atrioventricular septal defect in patients with and without Down's syndrome
-
Marino B. Complete atrioventricular septal defect in patients with and without Down's syndrome. Ann Thorac Surg 1994;57:1687-8.
-
(1994)
Ann Thorac Surg
, vol.57
, pp. 1687-1688
-
-
Marino, B.1
-
7
-
-
0035003429
-
Evaluation of prenatal diagnosis of associated congenital heart diseases by fetal ultrasonographic examination in Europe
-
EUROSCAN Study Group
-
Stoll C, Garne E, Clementi M. EUROSCAN Study Group. Evaluation of prenatal diagnosis of associated congenital heart diseases by fetal ultrasonographic examination in Europe. Prenat Diagn 2001;21:243-52.
-
(2001)
Prenat Diagn
, vol.21
, pp. 243-252
-
-
Stoll, C.1
Garne, E.2
Clementi, M.3
-
8
-
-
0027154167
-
Causes of congenital heart diseases: Old and new modes, mechanisms and models
-
Nora JJ. Causes of congenital heart diseases: old and new modes, mechanisms and models. Am Heart J 1993;125:1409-19.
-
(1993)
Am Heart J
, vol.125
, pp. 1409-1419
-
-
Nora, J.J.1
-
9
-
-
0001590320
-
Mechanisms in the pathogenesis of congenital heart defects
-
Pierpont ME, Moller JM, eds. Boston: Martinus-Nijoff
-
Clark EB. Mechanisms in the pathogenesis of congenital heart defects. In: Pierpont ME, Moller JM, eds. The genetics of cardiovascular diseases. Boston: Martinus-Nijoff, 1986:3-11.
-
(1986)
The Genetics of Cardiovascular Diseases
, pp. 3-11
-
-
Clark, E.B.1
-
10
-
-
1842413728
-
Holt-Oram syndrome is caused by mutations in TBX5 a member of the Brachyury (T) gene family
-
Li QY, Newbury-Ecob RA, Terrett JA, et al. Holt-Oram syndrome is caused by mutations in TBX5 a member of the Brachyury (T) gene family. Nat Genet 1997;15:21-9.
-
(1997)
Nat Genet
, vol.15
, pp. 21-29
-
-
Li, Q.Y.1
Newbury-Ecob, R.A.2
Terrett, J.A.3
-
11
-
-
0032479573
-
Congenital heart disease caused by mutations in the transcription factor NKX2-5
-
Schott JJ, Benson DW, Basson CT, et al. Congenital heart disease caused by mutations in the transcription factor NKX2-5. Science 1998;281:108-11.
-
(1998)
Science
, vol.281
, pp. 108-111
-
-
Schott, J.J.1
Benson, D.W.2
Basson, C.T.3
-
12
-
-
0034022637
-
Mutations in TFAP2B cause Char syndrome, a familial form of patent ductus areriosus
-
Satoda M, Zhao F, Diaz GA, et al. Mutations in TFAP2B cause Char syndrome, a familial form of patent ductus areriosus. Nat Genet 2000;25:42-6.
-
(2000)
Nat Genet
, vol.25
, pp. 42-46
-
-
Satoda, M.1
Zhao, F.2
Diaz, G.A.3
-
13
-
-
0034104297
-
Mutations in a new gene in Ellis-van Creveld syndrome and Weyers acrodental dysostosis
-
Ruiz-Perez VL, Ide SE, Strom TM, et al. Mutations in a new gene in Ellis-van Creveld syndrome and Weyers acrodental dysostosis. Nat Genet 2000;24:283-6.
-
(2000)
Nat Genet
, vol.24
, pp. 283-286
-
-
Ruiz-Perez, V.L.1
Ide, S.E.2
Strom, T.M.3
-
14
-
-
18344385476
-
Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome
-
Tartaglia M, Mehler EL, Goldberg R, et al. Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome. Nat Genet 2001;29:465-8.
-
(2001)
Nat Genet
, vol.29
, pp. 465-468
-
-
Tartaglia, M.1
Mehler, E.L.2
Goldberg, R.3
-
15
-
-
0033822768
-
X-linked transposition of the great arteries and incomplete penetrance among males with a nonsense mutation in ZIC3
-
Megarbane A, Salem N, Stephan E, et al. X-linked transposition of the great arteries and incomplete penetrance among males with a nonsense mutation in ZIC3. Eur J Hum Genet 2000;8:704-8.
-
(2000)
Eur J Hum Genet
, vol.8
, pp. 704-708
-
-
Megarbane, A.1
Salem, N.2
Stephan, E.3
-
16
-
-
0033598389
-
Congenital heart disease in mice deficient for the DiGeorge syndrome region
-
Lindsay EA, Botta A, Jurecic V, et al. Congenital heart disease in mice deficient for the DiGeorge syndrome region. Nature 1999;401:379-83.
-
(1999)
Nature
, vol.401
, pp. 379-383
-
-
Lindsay, E.A.1
Botta, A.2
Jurecic, V.3
-
17
-
-
0345636017
-
The incidence of pediatric cardiomyopathy in two regions of the United States
-
Lipshultz SE, Sleeper LA, Towbin JA, et al. The incidence of pediatric cardiomyopathy in two regions of the United States. N Engl J Med 2003;348:1647-55.
-
(2003)
N Engl J Med
, vol.348
, pp. 1647-1655
-
-
Lipshultz, S.E.1
Sleeper, L.A.2
Towbin, J.A.3
-
18
-
-
0032080504
-
Efficiency metabolic screening in childhood cardiomyopathies
-
Bonnet D, de Lonlay P, Gautier I, et al. Efficiency metabolic screening in childhood cardiomyopathies. Eur Heart J 1998;19:790-3.
-
(1998)
Eur Heart J
, vol.19
, pp. 790-793
-
-
Bonnet, D.1
De Lonlay, P.2
Gautier, I.3
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