-
1
-
-
0000846120
-
Familial heart disease and skeletal manifestations
-
Holt M, Oram S. Familial heart disease and skeletal manifestations. Br Heart J 1960;22:236-42.
-
(1960)
Br Heart J
, vol.22
, pp. 236-242
-
-
Holt, M.1
Oram, S.2
-
3
-
-
0005215398
-
Congenital heart disease and upper-extremity deformities. A report of two families
-
Holmes LB. Congenital heart disease and upper-extremity deformities. A report of two families. N Engl J Med 1965;272:437-44.
-
(1965)
N Engl J Med
, vol.272
, pp. 437-444
-
-
Holmes, L.B.1
-
6
-
-
0000724498
-
The upper limb-cardiovascular syndrome. An autosomal dominant genetic effect on embryogenesis
-
Lewis KB, Bruce RA, Baum D, Motulsky AG. The upper limb-cardiovascular syndrome. An autosomal dominant genetic effect on embryogenesis.JAMA 1965;193:1080-6.
-
(1965)
JAMA
, vol.193
, pp. 1080-1086
-
-
Lewis, K.B.1
Bruce, R.A.2
Baum, D.3
Motulsky, A.G.4
-
7
-
-
0028363797
-
Holt-Oram syndrome is a genetically heterogeneous disease with one locus mapping to human chromosome 12q
-
Terrett JA, Newbury-Ecob E, Cross GS, et al Holt-Oram syndrome is a genetically heterogeneous disease with one locus mapping to human chromosome 12q. Nature Genet 1994;6:401-4.
-
(1994)
Nature Genet
, vol.6
, pp. 401-404
-
-
Terrett, J.A.1
Newbury-Ecob, E.2
Cross, G.S.3
-
8
-
-
0013886180
-
Holt-Oram syndrome: Clinical and genetic study of a large family
-
Gall JC, Stern AM, Cohen MM, Adams MS, Davidson RT. Holt-Oram syndrome: clinical and genetic study of a large family. Am J Hum Genet 1966;18:187-200.
-
(1966)
Am J Hum Genet
, vol.18
, pp. 187-200
-
-
Gall, J.C.1
Stern, A.M.2
Cohen, M.M.3
Adams, M.S.4
Davidson, R.T.5
-
9
-
-
0020036143
-
Holt-Oram syndrome: Penetrance of the gene and lack of maternal effect
-
Gladstone I, Sybert VP. Holt-Oram syndrome: penetrance of the gene and lack of maternal effect. Clin Genet 1982;21:98-103.
-
(1982)
Clin Genet
, vol.21
, pp. 98-103
-
-
Gladstone, I.1
Sybert, V.P.2
-
11
-
-
0015978704
-
Anomalies associated with radial dysplasia
-
Carroll RE, Louis DS. Anomalies associated with radial dysplasia. J Pediatr 1974;84:409-11.
-
(1974)
J Pediatr
, vol.84
, pp. 409-411
-
-
Carroll, R.E.1
Louis, D.S.2
-
12
-
-
0026664519
-
Familial atrial septal defect with prolonged atrioventricular conduction
-
Bosi G, Sensi A, Calzolavi E, Scorrano M. Familial atrial septal defect with prolonged atrioventricular conduction. Am J Med Genet 1992;43:641.
-
(1992)
Am J Med Genet
, vol.43
, pp. 641
-
-
Bosi, G.1
Sensi, A.2
Calzolavi, E.3
Scorrano, M.4
-
13
-
-
0015428888
-
The upper limb cardiovascular syndrome
-
Brans YW, Lintermans JP. The upper limb cardiovascular syndrome. Am J Dis Child 1972;124:779-83.
-
(1972)
Am J Dis Child
, vol.124
, pp. 779-783
-
-
Brans, Y.W.1
Lintermans, J.P.2
-
14
-
-
0025282412
-
Heart-hand syndrome II. A report of Tabatznik syndrome with new findings
-
Silengo MC, Biagioli M, Guala A, Lopez-Bell G, Lala R. Heart-hand syndrome II. A report of Tabatznik syndrome with new findings. Clin Genet 1990;38:105-13.
-
(1990)
Clin Genet
, vol.38
, pp. 105-113
-
-
Silengo, M.C.1
Biagioli, M.2
Guala, A.3
Lopez-Bell, G.4
Lala, R.5
-
15
-
-
0018820469
-
Heart-hand syndrome III. A new syndrome in three generations
-
Ruiz De La Fuente S, Prieto F. Heart-hand syndrome III. A new syndrome in three generations. Hum Genet 1980;55:43-7.
-
(1980)
Hum Genet
, vol.55
, pp. 43-47
-
-
Ruiz De La Fuente, S.1
Prieto, F.2
-
17
-
-
0023158893
-
Thrombocytopenia and absent radius (TAR) syndrome
-
Hall JG. Thrombocytopenia and absent radius (TAR) syndrome. J Med Genet 1987;24:79-83.
-
(1987)
J Med Genet
, vol.24
, pp. 79-83
-
-
Hall, J.G.1
-
18
-
-
0020351041
-
Spectrum of anomalies in Fanconi anaemia
-
Glanz A, Fraser FC. Spectrum of anomalies in Fanconi anaemia. J Med Genet 1982;19:412-16.
-
(1982)
J Med Genet
, vol.19
, pp. 412-416
-
-
Glanz, A.1
Fraser, F.C.2
-
19
-
-
0020623203
-
A population study of the VACTERL association
-
Khoury MJ, Cordero JF, Greenberg F, James LM, Erickson JD. A population study of the VACTERL association. Pediatrics 1983;71:815-20.
-
(1983)
Pediatrics
, vol.71
, pp. 815-820
-
-
Khoury, M.J.1
Cordero, J.F.2
Greenberg, F.3
James, L.M.4
Erickson, J.D.5
-
20
-
-
19144363300
-
Holt-Oram syndrome
-
Chang CHJ. Holt-Oram syndrome. Radiology 1987;88:470-83.
-
(1987)
Radiology
, vol.88
, pp. 470-483
-
-
Chang, C.H.J.1
-
21
-
-
0028281469
-
The clinical and genetic spectrum of the Holt-Oram syndrome (heart-hand syndrome)
-
Basson CT, Cowley GS, Solomon SD, et al The clinical and genetic spectrum of the Holt-Oram syndrome (heart-hand syndrome). N Engl J Med 1994;330:885-91.
-
(1994)
N Engl J Med
, vol.330
, pp. 885-891
-
-
Basson, C.T.1
Cowley, G.S.2
Solomon, S.D.3
-
24
-
-
0020065640
-
Holt-Oram syndrome mistaken for thalidomide embryopathy - Embryological considerations
-
Van Regemorter N, Haumont D, Kirkpatrick C, et al. Holt-Oram syndrome mistaken for thalidomide embryopathy - embryological considerations. Eur J Pediatr 1982;138:77-80.
-
(1982)
Eur J Pediatr
, vol.138
, pp. 77-80
-
-
Van Regemorter, N.1
Haumont, D.2
Kirkpatrick, C.3
-
25
-
-
0013656160
-
The genetics of hand malformations
-
Temtamy SA, McKusick VA. The genetics of hand malformations. Birth Defects 1978;XIV(3):117-33.
-
(1978)
Birth Defects
, vol.14
, Issue.3
, pp. 117-133
-
-
Temtamy, S.A.1
McKusick, V.A.2
-
26
-
-
49749201562
-
Medical genetics
-
McKusick VA. Medical genetics. J Chronic Dis 1961;14:1-198.
-
(1961)
J Chronic Dis
, vol.14
, pp. 1-198
-
-
McKusick, V.A.1
-
27
-
-
0027538649
-
Retreat of the triplet repeat
-
Brook JD. Retreat of the triplet repeat. Nature Genet 1993;3:279-87.
-
(1993)
Nature Genet
, vol.3
, pp. 279-287
-
-
Brook, J.D.1
|