-
1
-
-
0017620817
-
Genetics of Möobius syndrome
-
Baraitser M. 1977. Genetics of Möobius syndrome. J Med Genet 14:415-417.
-
(1977)
J Med Genet
, vol.14
, pp. 415-417
-
-
Baraitser, M.1
-
2
-
-
77955283059
-
Moebius syndrome
-
Myrianthopoulos NC editor. Amsterdam: North Holland Publishing Co
-
Baraitser W. 1981. Moebius syndrome. In Myrianthopoulos NC editor. Neurogenetic directory part 1. Handbook of clinical neurology. Vol 42. Amsterdam: North Holland Publishing Co, p. 324-325.
-
(1981)
Neurogenetic Directory Part 1. Handbook of Clinical Neurology
, vol.42
, pp. 324-325
-
-
Baraitser, W.1
-
4
-
-
33646210828
-
Beitrag zur Lehere von den angeborenen beweglichkeitsdefekten im Bereich der Augen-Gesichtsund Schulter musculature (infantiler kernschwund Moebius)
-
Beetz P. 1913. Beitrag zur Lehere von den angeborenen beweglichkeitsdefekten im Bereich der Augen-Gesichtsund Schulter musculature (infantiler kernschwund Moebius). J Psychiatr Neurol 20:137-140.
-
(1913)
J Psychiatr Neurol
, vol.20
, pp. 137-140
-
-
Beetz, P.1
-
5
-
-
0022537899
-
Subclavian artery supply disruption sequence: Hypothesis of a vascular etiology for Poland, Klippel-Feil, and Möbius anomalies
-
Bouwes-Bavinck JN, Weaver DD. 1986. Subclavian artery supply disruption sequence: Hypothesis of a vascular etiology for Poland, Klippel-Feil, and Möbius anomalies. Am J Med Genet 23:903-918.
-
(1986)
Am J Med Genet
, vol.23
, pp. 903-918
-
-
Bouwes-Bavinck, J.N.1
Weaver, D.D.2
-
6
-
-
33745831247
-
Neuropsychiatric findings of Möbius sequence - A review
-
DOI 10.1111/j.1399-0004.2006.00649.x
-
Briegel W. 2006. Neuropsychiatric findings of Möbius sequence - A review. Clin Genet 70:91-97. (Pubitemid 44028094)
-
(2006)
Clinical Genetics
, vol.70
, Issue.2
, pp. 91-97
-
-
Briegel, W.1
-
7
-
-
0020405376
-
Moebius syndrome in a child and extremity defect in her father
-
Collins DL, Schimke RN. 1982. Moebius syndrome in a child and extremity defect in her father. Clin Genet 22:312-314.
-
(1982)
Clin Genet
, vol.22
, pp. 312-314
-
-
Collins, D.L.1
Schimke, R.N.2
-
8
-
-
0033615402
-
Möbius sequence, hypogenitalism, cerebral, and skeletal malformations in two brothers
-
Criado GR, Perez Aytes A. 1999. Möbius sequence, hypogenitalism, cerebral, and skeletal malformations in two brothers. Am J Med Genet 86:492-496.
-
(1999)
Am J Med Genet
, vol.86
, pp. 492-496
-
-
Criado, G.R.1
Perez Aytes, A.2
-
9
-
-
0027335547
-
Broad-spectrum Mobius syndrome associated with a 1;11 chromosome translocation
-
Donahue S, Wenger S, Steele M, Gorin M. 1993. Broad-spectrum Möbius syndrome associated with a 1;11 chromosome translocation. Ophthalmic Paediatr Genet 14:17-21. (Pubitemid 23143869)
-
(1993)
Ophthalmic Paediatrics and Genetics
, vol.14
, Issue.1
, pp. 17-21
-
-
Donahue, S.P.1
Wenger, S.L.2
Steele, M.W.3
Gorin, M.B.4
-
11
-
-
0008567319
-
Congenital paralysis of lateral rotators of eyes with paralysis of muscles of face
-
Hicks AM. 1943. Congenital paralysis of lateral rotators of eyes with paralysis of muscles of face. Arch Ophthalmol 30:38-42.
-
(1943)
Arch Ophthalmol
, vol.30
, pp. 38-42
-
-
Hicks, A.M.1
-
12
-
-
0024811772
-
MCA/MR syndrome with oligodactyly and Möbius anomaly in first cousins: New syndrome or familial facial-limb disruption sequence?
-
Journel H, Roussey M, Le Marec B. 1989. MCA/MR syndrome with oligodactyly and Möbius anomaly in first cousins: New syndrome or familial facial-limb disruption sequence? Am J Med Genet 34:506-510.
-
(1989)
Am J Med Genet
, vol.34
, pp. 506-510
-
-
Journel, H.1
Roussey, M.2
Le Marec, B.3
-
13
-
-
0029658309
-
Localization of a gene for Mobius syndrome to chromosome 3q by linkage analysis in a Dutch family
-
DOI 10.1093/hmg/5.9.1367
-
Kremer H, Kuyt LP, van den Helm B, van Reen M, Leunissen JAM, Hamel BC, Jansen C, Mariman EC, Frants RR, Padberg GW. 1996. Localization of a gene for Möbius syndrome to chromosome 3q by linkage analysis in a Dutch family. Hum Mol Genet 5:1367-1371. (Pubitemid 26335857)
-
(1996)
Human Molecular Genetics
, vol.5
, Issue.9
, pp. 1367-1371
-
-
Kremer, H.1
Kuyt, L.P.2
Van Den Helm, B.3
Van Reen, M.4
Leunissen, J.A.M.5
Hamel, B.C.J.6
Jansen, C.7
Mariman, E.C.M.8
Frants, R.R.9
Padberg, G.W.10
-
14
-
-
0025122294
-
Moebius syndrome
-
Kumar D. 1990. Moebius syndrome. J Med Genet 27:122-126.
-
(1990)
J Med Genet
, vol.27
, pp. 122-126
-
-
Kumar, D.1
-
15
-
-
0019777410
-
Heterogeneity and pleiotropism in the Moebius syndrome
-
Legum C, Godel V, Nemet P. 1981. Heterogeneity and pleiotropism in the Moebius syndrome. Clin Genet 20:254-259.
-
(1981)
Clin Genet
, vol.20
, pp. 254-259
-
-
Legum, C.1
Godel, V.2
Nemet, P.3
-
16
-
-
0026026924
-
Oculofacial-bulbar palsy in mother and son: Review of 26 reports of familial transmission within the "Möbius spectrum of defects"
-
MacDermot KD, Winter RM, Taylor D, Baraitser M. 1990. Oculofacial-bulbar palsy in mother and son: Review of 26 reports of familial transmission within the "Möbius spectrum of defects". J Med Genet 27:18-26.
-
(1990)
J Med Genet
, vol.27
, pp. 18-26
-
-
MacDermot, K.D.1
Winter, R.M.2
Taylor, D.3
Baraitser, M.4
-
17
-
-
0021035698
-
Facial weakness in oligosyndactyly: 2 independent variable features of familial type of the Möbius syndrome
-
Mitter NS, Chudley AE. 1983. Facial weakness in oligosyndactyly: 2 independent variable features of familial type of the Möbius syndrome. Clin Genet 24:350-354.
-
(1983)
Clin Genet
, vol.24
, pp. 350-354
-
-
Mitter, N.S.1
Chudley, A.E.2
-
19
-
-
0030610414
-
Mobius-like syndrome associated with a 1;2 chromosome translocation
-
Nishikawa M, Ichiyama T, Hayashi T, Furukawa S. 1997. Mobius-like syndrome associated with a 1;2 chromosome translocation. Clin Genet 51:122-123. (Pubitemid 27149721)
-
(1997)
Clinical Genetics
, vol.51
, Issue.2
, pp. 122-123
-
-
Nishikawa, M.1
Ichiyama, T.2
Hayashi, T.3
Furukawa, S.4
-
20
-
-
0040920369
-
-
McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University (Baltimore, MD) and Bethesda, MD: National Library of Medicine. World Wide Web
-
Online Mendelian Inheritance in Man, OMIM (TM). 2007. McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University (Baltimore, MD) and National Center for Biotechnology Information. Bethesda, MD: National Library of Medicine. World Wide Web URL: http://www.ncbi.nlm.nih.gov/omim/.
-
(2007)
Online Mendelian Inheritance in Man, OMIM (TM)
-
-
-
21
-
-
0026635047
-
Möbius syndrome with basal ganglia calcification
-
Singh B, Shahwan SA, Singh P, Al Deeb SM, Sharif H. 1992. Möbius syndrome with basal ganglia calcification. Acta Neurol Scand 85:436-438.
-
(1992)
Acta Neurol Scand
, vol.85
, pp. 436-438
-
-
Singh, B.1
Shahwan, S.A.2
Singh, P.3
Al Deeb, S.M.4
Sharif, H.5
-
22
-
-
0025884458
-
Deletion of chromosome 13 in Moebius syndrome
-
Slee J, Smart R, Viljoen D. 1991. Deletion of chromosome 13 in Moebius syndrome. J Med Genet 28:413-414.
-
(1991)
J Med Genet
, vol.28
, pp. 413-414
-
-
Slee, J.1
Smart, R.2
Viljoen, D.3
-
23
-
-
1842368241
-
Congenital facial paralysis
-
Thomas HM. 1898. Congenital facial paralysis. J Nerv Ment Dis 25:571-593.
-
(1898)
J Nerv Ment Dis
, vol.25
, pp. 571-593
-
-
Thomas, H.M.1
-
24
-
-
0019582235
-
Fetal vascular disruptions: Mechanisms and some resulting birth defects
-
Van Allen MI. 1981. Fetal vascular disruptions: Mechanisms and some resulting birth defects. Pediatr Ann 10:219-233.
-
(1981)
Pediatr Ann
, vol.10
, pp. 219-233
-
-
Van Allen, M.I.1
-
26
-
-
0033364729
-
A second gene for autosomal dominant mobius syndrome is localized to chromosome 10q, in a Dutch family
-
DOI 10.1086/302539
-
Verzijl HT, van den Helm B, Veldman B, Hamel BC, Kuyt LP, Padberg GW, Kremer H. 1999. A second gene for autosomal dominant Möbius syndrome is localized to chromosome 10q, in a Dutch family. Am J Hum Genet 65:752-756. (Pubitemid 30468720)
-
(1999)
American Journal of Human Genetics
, vol.65
, Issue.3
, pp. 752-756
-
-
Verzijl, H.T.F.M.1
Van Den Helm, B.2
Veldman, B.3
Hamel, B.C.J.4
Kuyt, L.P.5
Padberg, G.W.6
Kremer, H.7
-
27
-
-
0017626152
-
Three generation pedigree of a Mobius syndrome variant with chromosome translocation
-
Ziter F, Wiser W, Robinson A. 1977. Three-generation pedigree of a Möbius syndrome variant with chromosome translocation. Arch Neurol 34:437-442. (Pubitemid 8141204)
-
(1977)
Archives of Neurology
, vol.34
, Issue.7
, pp. 437-442
-
-
Ziter, F.A.1
Wiser, W.C.2
Robinson, A.3
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