-
1
-
-
0025373428
-
Congenital heart disease: Incidence and inheritance
-
Hoffman JIE. Congenital heart disease: incidence and inheritance. Pediatr Clin North Am. 1990;37:25-43.
-
(1990)
Pediatr Clin North Am
, vol.37
, pp. 25-43
-
-
Hoffman, J.I.E.1
-
2
-
-
0008348113
-
Atrial septal defect secundum
-
Fyler DC, ed. Boston, Mass: Mosby Year Book, Inc
-
Fyler DC. Atrial septal defect secundum. In: Fyler DC, ed. Nadas' Pediatric Cardiology. Boston, Mass: Mosby Year Book, Inc; 1992: 513-524.
-
(1992)
Nadas' Pediatric Cardiology
, pp. 513-524
-
-
Fyler, D.C.1
-
3
-
-
0344468294
-
Embryology of the atrioventricular canal region and pathogenesis of endocardial cushion defects
-
Feldt RH, McGoon DC, Ongley PA, Rastelli GC, Titus JL, Van Mierop LHS, eds. Philadelphia, Pa: WB Saunders
-
Van Mierop LHS. Embryology of the atrioventricular canal region and pathogenesis of endocardial cushion defects. In: Feldt RH, McGoon DC, Ongley PA, Rastelli GC, Titus JL, Van Mierop LHS, eds. Atrioventricular Canal Defects. Philadelphia, Pa: WB Saunders; 1976:1-12.
-
(1976)
Atrioventricular Canal Defects
, pp. 1-12
-
-
Van Mierop, L.H.S.1
-
4
-
-
84920308417
-
-
Online Mendelian Inheritance in Man, OMIM (TM). Baltimore, Md: Johns Hopkins University
-
Online Mendelian Inheritance in Man, OMIM (TM). Baltimore, Md: Johns Hopkins University; World Wide Web URL:http://www3.ncbi.nlm.nih.gov/omim/.
-
-
-
-
5
-
-
0023201719
-
Familial risks of congenital heart defect assessed in a population based epidemiologic study
-
Boughman JA, Berg KA, Astemberski JA, Clark EB, McCarter RJ, Rubin JD, Ferencz C. Familial risks of congenital heart defect assessed in a population based epidemiologic study. Am J Med Genet. 1987;26: 839-849.
-
(1987)
Am J Med Genet
, vol.26
, pp. 839-849
-
-
Boughman, J.A.1
Berg, K.A.2
Astemberski, J.A.3
Clark, E.B.4
McCarter, R.J.5
Rubin, J.D.6
Ferencz, C.7
-
6
-
-
0028239319
-
A second-generation study of 427 probands with congenital heart defects and their 837 children
-
Whittemore R, Wells JA, Castellsague X. A second-generation study of 427 probands with congenital heart defects and their 837 children. J Am Coll Cardiol. 1994;23:1459-1467.
-
(1994)
J Am Coll Cardiol
, vol.23
, pp. 1459-1467
-
-
Whittemore, R.1
Wells, J.A.2
Castellsague, X.3
-
7
-
-
0022344130
-
Diagnosis and classification of atrial septal aneurysm by two-dimensional echocardiography: Report of 80 consecutive cases
-
Hanley PC, Tajik AJ, Hynes JK, Edwards WD, Reeder GS, Hagler DJ, Seward JB. Diagnosis and classification of atrial septal aneurysm by two-dimensional echocardiography: report of 80 consecutive cases. J Am Coll Cardiol. 1985;6:1370-1382.
-
(1985)
J Am Coll Cardiol
, vol.6
, pp. 1370-1382
-
-
Hanley, P.C.1
Tajik, A.J.2
Hynes, J.K.3
Edwards, W.D.4
Reeder, G.S.5
Hagler, D.J.6
Seward, J.B.7
-
8
-
-
0024465523
-
Natural course of atrial septal aneurysm in children and the potential for spontaneous closure of associated septal defect
-
Brand A, Keren A, Branski D, Abrahamov A, Stern S. Natural course of atrial septal aneurysm in children and the potential for spontaneous closure of associated septal defect. Am J Cardiol. 1989;64:996-1001.
-
(1989)
Am J Cardiol
, vol.64
, pp. 996-1001
-
-
Brand, A.1
Keren, A.2
Branski, D.3
Abrahamov, A.4
Stern, S.5
-
9
-
-
0025164036
-
A molecular basis for familial hypertrophic cardiomyopathy: An α/β cardiac myosin heavy chain hybrid gene
-
Tanigawa G, Jarcho JA, Kass S, Solomon SD, Vosberg H-P, Seidman JG, Seidman CE. A molecular basis for familial hypertrophic cardiomyopathy: an α/β cardiac myosin heavy chain hybrid gene. Cell. 1990;62: 991-998.
-
(1990)
Cell
, vol.62
, pp. 991-998
-
-
Tanigawa, G.1
Jarcho, J.A.2
Kass, S.3
Solomon, S.D.4
Vosberg, H.-P.5
Seidman, J.G.6
Seidman, C.E.7
-
10
-
-
0014832506
-
Anatomically isolated aortic valvular disease: The case against its being of rheumatic etiology
-
Roberts WC. Anatomically isolated aortic valvular disease: the case against its being of rheumatic etiology. Am J Med. 1970;49: 151-159.
-
(1970)
Am J Med
, vol.49
, pp. 151-159
-
-
Roberts, W.C.1
-
11
-
-
0017235209
-
Familial atrial septal defect with prolonged atrioventricular conduction
-
Pease WE, Nordenberg A, Ladda RL. Familial atrial septal defect with prolonged atrioventricular conduction. Circulation. 1976;53:759-762.
-
(1976)
Circulation
, vol.53
, pp. 759-762
-
-
Pease, W.E.1
Nordenberg, A.2
Ladda, R.L.3
-
12
-
-
0028910750
-
Genetic heterogeneity of heart-hand syndromes
-
Basson CT, Solomon SD, Weissman B, MacRae CA, Poznanski AK, Prieto F, de la Fuente SR, Pease WE, Levin SE, Holmes LB, Seidman JG, Seidman CE. Genetic heterogeneity of heart-hand syndromes. Circulation. 1995;91:1326-1329.
-
(1995)
Circulation
, vol.91
, pp. 1326-1329
-
-
Basson, C.T.1
Solomon, S.D.2
Weissman, B.3
MacRae, C.A.4
Poznanski, A.K.5
Prieto, F.6
De la Fuente, S.R.7
Pease, W.E.8
Levin, S.E.9
Holmes, L.B.10
Seidman, J.G.11
Seidman, C.E.12
-
13
-
-
0018669834
-
Venous anomalies of the coronary sinus: Detection by M-mode, two-dimensional and contrast echocardiography
-
Snider AR, Ports TA, Silverman NH. Venous anomalies of the coronary sinus: detection by M-mode, two-dimensional and contrast echocardiography. Circulation. 1979;60:721-727.
-
(1979)
Circulation
, vol.60
, pp. 721-727
-
-
Snider, A.R.1
Ports, T.A.2
Silverman, N.H.3
-
14
-
-
0014820336
-
The congenitally bicuspid aortic valve: A study of 85 autopsy patients
-
Roberts WC. The congenitally bicuspid aortic valve: a study of 85 autopsy patients. Am J Cardiol. 1970;26:72-83.
-
(1970)
Am J Cardiol
, vol.26
, pp. 72-83
-
-
Roberts, W.C.1
-
15
-
-
0026071709
-
Superiority of transesophageal echocardiography in detecting cardiac source of embolization in patients with cerebral ischemia of uncertain etiology
-
Pearson AC, Labovitz AJ, Tatineni S, Gomez CR. Superiority of transesophageal echocardiography in detecting cardiac source of embolization in patients with cerebral ischemia of uncertain etiology. J Am Coll Cardiol. 1991;17:66-72.
-
(1991)
J Am Coll Cardiol
, vol.17
, pp. 66-72
-
-
Pearson, A.C.1
Labovitz, A.J.2
Tatineni, S.3
Gomez, C.R.4
-
16
-
-
0021061381
-
Spontaneous closure of secundum atrial septal defect in infants and young children
-
Cockerham JT, Martin TC, Gutierrez FR, Hartman AF Jr, Goldring D, Strauss AW. Spontaneous closure of secundum atrial septal defect in infants and young children. Am J Cardiol. 1983;52:1267-1271.
-
(1983)
Am J Cardiol
, vol.52
, pp. 1267-1271
-
-
Cockerham, J.T.1
Martin, T.C.2
Gutierrez, F.R.3
Hartman A.F., Jr.4
Goldring, D.5
Strauss, A.W.6
-
17
-
-
0028813979
-
A gene for familial total anomalous pulmonary venous return maps to chromosome 4p13-q12
-
Bleyl S, Nelson L, Odelberg SJ, Ruttenberg HD, Otterud B, Leppert M, Ward K. A gene for familial total anomalous pulmonary venous return maps to chromosome 4p13-q12. Am J Hum Genet. 1995;56:408-415.
-
(1995)
Am J Hum Genet
, vol.56
, pp. 408-415
-
-
Bleyl, S.1
Nelson, L.2
Odelberg, S.J.3
Ruttenberg, H.D.4
Otterud, B.5
Leppert, M.6
Ward, K.7
-
18
-
-
0031022393
-
Identification of a complex congenital heart defect susceptibility locus by using DNA pooling and shared segment analysis
-
Sheffield VC, Pierpont ME, Nishimura D, Beck JS, Burns TL, Berg MA, Stone EM, Patil SR, Lauer RM. Identification of a complex congenital heart defect susceptibility locus by using DNA pooling and shared segment analysis. Hum Mol Genet. 1997;6:117-121.
-
(1997)
Hum Mol Genet
, vol.6
, pp. 117-121
-
-
Sheffield, V.C.1
Pierpont, M.E.2
Nishimura, D.3
Beck, J.S.4
Burns, T.L.5
Berg, M.A.6
Stone, E.M.7
Patil, S.R.8
Lauer, R.M.9
-
19
-
-
0008304448
-
Familial congenital heart disease: Familial occurrence of atrial septal defect with A-V conduction abnormalities: supravalvular aortic and pulmonic stenosis; and ventricular septal defect
-
Kahler RL, Braunwald E, Plauth WH Jr, Morrow AG. Familial congenital heart disease: familial occurrence of atrial septal defect with A-V conduction abnormalities: supravalvular aortic and pulmonic stenosis; and ventricular septal defect. Am J Med. 1966;40:384-399.
-
(1966)
Am J Med
, vol.40
, pp. 384-399
-
-
Kahler, R.L.1
Braunwald, E.2
Plauth W.H., Jr.3
Morrow, A.G.4
-
20
-
-
0015165538
-
Dominant mode of inheritance in atrial septal defect
-
Zetterqvist P, Turesson I, Johansson BW, Laurell S, Ohlsson N-M. Dominant mode of inheritance in atrial septal defect. Clin Genet. 1971; 2:78-86.
-
(1971)
Clin Genet
, vol.2
, pp. 78-86
-
-
Zetterqvist, P.1
Turesson, I.2
Johansson, B.W.3
Laurell, S.4
Ohlsson, N.-M.5
-
21
-
-
0014769440
-
Familial atrial septal defect with prolonged atrioventricular conduction: A syndrome showing the autosomal dominant pattern of inheritance
-
Bizarro RO, Callahan JA, Feldt RH, Kurland LT, Gordon H, Brandenburg RO. Familial atrial septal defect with prolonged atrioventricular conduction: a syndrome showing the autosomal dominant pattern of inheritance. Circulation. 1970;41:677-683.
-
(1970)
Circulation
, vol.41
, pp. 677-683
-
-
Bizarro, R.O.1
Callahan, J.A.2
Feldt, R.H.3
Kurland, L.T.4
Gordon, H.5
Brandenburg, R.O.6
-
23
-
-
0018377872
-
Gemeinsame Mechanismen der Mißbildungsentstehung beim erblichen und sporadischen Vorhofseptumdefekt Typ II
-
Mohl W, Mayr WR, Hauser G, Reuer E, Wimmer M, Herbich J. Gemeinsame Mechanismen der Mißbildungsentstehung beim erblichen und sporadischen Vorhofseptumdefekt Typ II. Wien Klin Wochenschr. 1979;91:307-314.
-
(1979)
Wien Klin Wochenschr
, vol.91
, pp. 307-314
-
-
Mohl, W.1
Mayr, W.R.2
Hauser, G.3
Reuer, E.4
Wimmer, M.5
Herbich, J.6
-
24
-
-
0025739475
-
Autosomal dominant atrial septal defect of ostium secundum type
-
Li Volti S, Distefano G, Garozzo R, Romeo MG, Sciacca P, Mollica F. Autosomal dominant atrial septal defect of ostium secundum type. Ann Genet. 1991;34:14-18.
-
(1991)
Ann Genet
, vol.34
, pp. 14-18
-
-
Li Volti, S.1
Distefano, G.2
Garozzo, R.3
Romeo, M.G.4
Sciacca, P.5
Mollica, F.6
-
25
-
-
0028281469
-
The clinical and genetic spectrum of the Holt-Oram syndrome (heart-hand syndrome)
-
Basson CT, Cowley GS, Solomon SD, Weissman B, Poznanski AK, Traill TA, Seidman JG, Seidman CE. The clinical and genetic spectrum of the Holt-Oram syndrome (heart-hand syndrome). N Engl J Med. 1994;330:885-891.
-
(1994)
N Engl J Med
, vol.330
, pp. 885-891
-
-
Basson, C.T.1
Cowley, G.S.2
Solomon, S.D.3
Weissman, B.4
Poznanski, A.K.5
Traill, T.A.6
Seidman, J.G.7
Seidman, C.E.8
-
27
-
-
0030636780
-
Mutations in human TBX5 cause limb and cardiac malformation in Holt-Oram syndrome
-
Basson CT, Bachinsky DR, Lin RC, Levi T, Elkins JA, Soults J, Grayzel D, Kroumpouzou E, Traill TA, Leblanc-Straceski J, Renault B, Kucherlapati R, Seidman JG, Seidman CE. Mutations in human TBX5 cause limb and cardiac malformation in Holt-Oram syndrome. Nat Genet. 1997;15: 30-35.
-
(1997)
Nat Genet
, vol.15
, pp. 30-35
-
-
Basson, C.T.1
Bachinsky, D.R.2
Lin, R.C.3
Levi, T.4
Elkins, J.A.5
Soults, J.6
Grayzel, D.7
Kroumpouzou, E.8
Traill, T.A.9
Leblanc-Straceski, J.10
Renault, B.11
Kucherlapati, R.12
Seidman, J.G.13
Seidman, C.E.14
-
28
-
-
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, Wilson DI, Curtis ARJ, Yi CH, Gebuhr T, Bullen PJ, Robson SC, Strachan T, Bonnet D, Lyonnet S, Young ID, Raeburn JA, Buckler AJ, Laaw DJ, Brook JD. Holt-Oram syndrome is caused by mutations in TBX5 a member of the Brachyury (T) gene family. Nat Genet. 1997;15:21-29.
-
(1997)
Nat Genet
, vol.15
, pp. 21-29
-
-
Li, Q.Y.1
Newbury-Ecob, R.A.2
Terrett, J.A.3
Wilson, D.I.4
Curtis, A.R.J.5
Yi, C.H.6
Gebuhr, T.7
Bullen, P.J.8
Robson, S.C.9
Strachan, T.10
Bonnet, D.11
Lyonnet, S.12
Young, I.D.13
Raeburn, J.A.14
Buckler, A.J.15
Laaw, D.J.16
Brook, J.D.17
-
29
-
-
0029994247
-
New understandings in the genetics of congenital heart disease
-
Benson DW, Basson CT, MacRae CA. New understandings in the genetics of congenital heart disease. Curr Opin Pediatr. 1996;8:505-511.
-
(1996)
Curr Opin Pediatr
, vol.8
, pp. 505-511
-
-
Benson, D.W.1
Basson, C.T.2
MacRae, C.A.3
-
30
-
-
0029780320
-
RXRα deficiency confers genetic susceptibility for aortic sac, conotruncal, atrioventricular cushion, and ventricular muscle defects in mice
-
Gruber PJ, Kubalak SW, Pexieder T, Sucov HM, Evans RM, Chien KR. RXRα deficiency confers genetic susceptibility for aortic sac, conotruncal, atrioventricular cushion, and ventricular muscle defects in mice. J Clin Invest. 1996;98:1332-1343.
-
(1996)
J Clin Invest
, vol.98
, pp. 1332-1343
-
-
Gruber, P.J.1
Kubalak, S.W.2
Pexieder, T.3
Sucov, H.M.4
Evans, R.M.5
Chien, K.R.6
-
31
-
-
0028941443
-
Five novel genes from the cri-du-chat critical region isolated by direct selection
-
Simmons AD, Goodart SA, Gallardo TD, Overhauser J, Lovett M. Five novel genes from the cri-du-chat critical region isolated by direct selection. Hum Mol Genet. 1995;4:295-302.
-
(1995)
Hum Mol Genet
, vol.4
, pp. 295-302
-
-
Simmons, A.D.1
Goodart, S.A.2
Gallardo, T.D.3
Overhauser, J.4
Lovett, M.5
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