-
1
-
-
0000541216
-
The congenital facial diplegia syndrome
-
Henderson JL. The congenital facial diplegia syndrome. Brain. 1939;62:381.
-
(1939)
Brain
, vol.62
, pp. 381
-
-
Henderson, J.L.1
-
2
-
-
0000207383
-
Mobius syndrome. A study and report of 18 cases
-
Amaya LG, Walker J, Taylor D. Mobius syndrome. A study and report of 18 cases. Binoc Vis. 1990;5:119-132.
-
(1990)
Binoc Vis
, vol.5
, pp. 119-132
-
-
Amaya, L.G.1
Walker, J.2
Taylor, D.3
-
4
-
-
0024347346
-
Moebius syndrome with unilateral cerebellar hypoplasia
-
Harbord MG, Ginn JP, Hall-Craggs MA. Moebius syndrome with unilateral cerebellar hypoplasia. J Med Genet. 1989;26:579-582.
-
(1989)
J Med Genet
, vol.26
, pp. 579-582
-
-
Harbord, M.G.1
Ginn, J.P.2
Hall-Craggs, M.A.3
-
5
-
-
0024449115
-
Moebius syndrome: Animal model-human correlations and evidence for a brainstem vascular etiology
-
Lipson AH, Webster WS, Brown-Woodman PDC, et al. Moebius syndrome: Animal model-human correlations and evidence for a brainstem vascular etiology. Teratology. 1989;40:339-350.
-
(1989)
Teratology
, vol.40
, pp. 339-350
-
-
Lipson, A.H.1
Webster, W.S.2
Brown-Woodman, P.D.C.3
-
6
-
-
0015953835
-
A family with Moebius syndrome
-
Becker CF, Lund N. A family with Moebius syndrome. J Pediatr. 1974;84:115.
-
(1974)
J Pediatr
, vol.84
, pp. 115
-
-
Becker, C.F.1
Lund, N.2
-
9
-
-
0024811772
-
MCA/MR syndrome with oligodactyly and Mobius anomaly in first cousins: New syndrome or familial facial-limb disruption sequence?
-
Journel H, Roussey M, Le Marec B. MCA/MR syndrome with oligodactyly and Mobius anomaly in first cousins: New syndrome or familial facial-limb disruption sequence? Am J Med Genet. 1989;34:506-510.
-
(1989)
Am J Med Genet
, vol.34
, pp. 506-510
-
-
Journel, H.1
Roussey, M.2
Le Marec, B.3
-
10
-
-
0025884458
-
Deletion of chromosome 13 in Mobius syndrome
-
Slee JJ, Smart RD, Vilijoen DL. Deletion of chromosome 13 in Mobius syndrome. J Med Genet. 1991;28:413-414.
-
(1991)
J Med Genet
, vol.28
, pp. 413-414
-
-
Slee, J.J.1
Smart, R.D.2
Vilijoen, D.L.3
-
11
-
-
0027335547
-
Broad-spectrum Mobius syndrome associated with a 1;11 chromosome translocation
-
Donahue SP, Wenger SL, Steele MW, et al. Broad-spectrum Mobius syndrome associated with a 1;11 chromosome translocation. Ophthalmic Paediatr Genet. 1993;14:17-21.
-
(1993)
Ophthalmic Paediatr Genet
, vol.14
, pp. 17-21
-
-
Donahue, S.P.1
Wenger, S.L.2
Steele, M.W.3
-
12
-
-
0030610414
-
Mobius-like syndrome associated with 1;2 chromosome translocation
-
Nishikawa M, Ichiyama T, Hayashi T, et al. Mobius-like syndrome associated with 1;2 chromosome translocation. Clin Genet. 1997;51:122-123.
-
(1997)
Clin Genet
, vol.51
, pp. 122-123
-
-
Nishikawa, M.1
Ichiyama, T.2
Hayashi, T.3
-
13
-
-
0029658309
-
Localization of a gene for Mobius syndrome to chromosome 3q by linkage analysis in a Dutch family
-
Kremer H, Kuyt LP, Helm B, et al. Localization of a gene for Mobius syndrome to chromosome 3q by linkage analysis in a Dutch family. Hum Mol Genet. 1996;5:1367-1371.
-
(1996)
Hum Mol Genet
, vol.5
, pp. 1367-1371
-
-
Kremer, H.1
Kuyt, L.P.2
Helm, B.3
-
14
-
-
0033364729
-
A second gene for autosomal dominant Mobius syndrome is localized to chromosome 10q, in a Dutch family
-
Verzijl HTFM, Van den Helm B, Veldman B, et al. A second gene for autosomal dominant Mobius syndrome is localized to chromosome 10q, in a Dutch family. Am J Hum Genet. 1999;65:752-756.
-
(1999)
Am J Hum Genet
, vol.65
, pp. 752-756
-
-
Verzijl, H.T.F.M.1
Van den Helm, B.2
Veldman, B.3
-
15
-
-
0003436550
-
-
Baltimore: Johns Hopkins University Press
-
th ed. Baltimore: Johns Hopkins University Press; 1998.
-
(1998)
th Ed.
-
-
McKusick, V.A.1
|