-
1
-
-
0033364729
-
A second gene for autosomal dominant Mobius syndrome is localized to chromosome 10q, in a Dutch family
-
Verzijl HT, van den Helm B, Veldman B, Hamel BC, Kuyt LP, Padberg GW, Kremer H. A second gene for autosomal dominant Mobius syndrome is localized to chromosome 10q, in a Dutch family. Am Hum Genet 1999;65:752-756.
-
(1999)
Am Hum Genet
, vol.65
, pp. 752-756
-
-
Verzijl, H.T.1
Van Den Helm, B.2
Veldman, B.3
Hamel, B.C.4
Kuyt, L.P.5
Padberg, G.W.6
Kremer, H.7
-
2
-
-
0024478267
-
A smile for the Mobius' syndrome patient
-
Zuker RM, Manktelow RT. A smile for the Mobius' syndrome patient. Ann Plast Surg 1989;22:188-194.
-
(1989)
Ann Plast Surg
, vol.22
, pp. 188-194
-
-
Zuker, R.M.1
Manktelow, R.T.2
-
3
-
-
0023153525
-
Variants of Mobius' syndrome and central neurologic impairment: Lindeman procedure in children
-
Cohen SR, Thompson JW. Variants of Mobius' syndrome and central neurologic impairment: Lindeman procedure in children. Ann Otol Rhinol Laryngol 1987;96:93-100.
-
(1987)
Ann Otol Rhinol Laryngol
, vol.96
, pp. 93-100
-
-
Cohen, S.R.1
Thompson, J.W.2
-
5
-
-
0020005003
-
Mobius-like syndrome due to multiple cerebral abnormalities including hypoplasia of the descending tracts. A case report
-
Nardelli E, Vio M, Ghersini L, Rizzuto N. Mobius-like syndrome due to multiple cerebral abnormalities including hypoplasia of the descending tracts. A case report. J Neurol 1982;227:11-19.
-
(1982)
J Neurol
, vol.227
, pp. 11-19
-
-
Nardelli, E.1
Vio, M.2
Ghersini, L.3
Rizzuto, N.4
-
6
-
-
0033172988
-
The Mobius sequence: A relook
-
Miller MT, Stromland K. The Mobius sequence: a relook. J AAPOS 1999;3:199-208.
-
(1999)
J AAPOS
, vol.3
, pp. 199-208
-
-
Miller, M.T.1
Stromland, K.2
-
7
-
-
0018331062
-
Pathophysiological effects of Mobius syndrome on speech and hearing
-
Kahane JC. Pathophysiological effects of Mobius syndrome on speech and hearing. Arch Otolaryngol 1979;105:29-34.
-
(1979)
Arch Otolaryngol
, vol.105
, pp. 29-34
-
-
Kahane, J.C.1
-
8
-
-
0025191855
-
The syndrome of Mobius sequence, peripheral neuropathy, and hypogonadotrophic hypogonadism
-
Kawai M, Momoi T, Fujii T, Nakano S, Itagald Y, Mikawa H. The syndrome of Mobius sequence, peripheral neuropathy, and hypogonadotrophic hypogonadism. Am J Med Genetic 1990;37:578-582.
-
(1990)
Am J Med Genetic
, vol.37
, pp. 578-582
-
-
Kawai, M.1
Momoi, T.2
Fujii, T.3
Nakano, S.4
Itagald, Y.5
Mikawa, H.6
-
9
-
-
0029658309
-
Localization of a gene for Mobius syndrome to chromosome 3q by linkage analysis in a Dutch family
-
Kremer H, Kuyt LP, van dem Helm B, van Reen M, Leunissin JA, Hamel BC, 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
Van Dem Helm, B.3
Van Reen, M.4
Leunissin, J.A.5
Hamel, B.C.6
-
10
-
-
0034996321
-
Autistic disorders in Mobius sequence: A comprehensive study of 25 individuals
-
Johansson M, Wentz E, Fernell E, Stromland K, Miller MT, Gillberg C. Autistic disorders in Mobius sequence: a comprehensive study of 25 individuals. Dev Med Child Neurol 2001;43:338-345.
-
(2001)
Dev Med Child Neurol
, vol.43
, pp. 338-345
-
-
Johansson, M.1
Wentz, E.2
Fernell, E.3
Stromland, K.4
Miller, M.T.5
Gillberg, C.6
-
12
-
-
0021675906
-
Childhood psychosis in a case of Moebius syndrome
-
Gillberg C, Winndergard I. Childhood psychosis in a case of Moebius syndrome. Neuropediatrics 1984;15:147-149.
-
(1984)
Neuropediatrics
, vol.15
, pp. 147-149
-
-
Gillberg, C.1
Winndergard, I.2
-
13
-
-
0021365416
-
Defective response to social cues in Mobius' syndrome
-
Giannini AJ, Tamulonis D, Giannini MC, Loiselle RH, Spirtos G. Defective response to social cues in Mobius' syndrome. J Nerv Ment Dis 1984;173:174-175.
-
(1984)
J Nerv Ment Dis
, vol.173
, pp. 174-175
-
-
Giannini, A.J.1
Tamulonis, D.2
Giannini, M.C.3
Loiselle, R.H.4
Spirtos, G.5
-
14
-
-
0030896761
-
Uterine contraction in the development of Mobius syndrome
-
Graf WD, Shepard TH. Uterine contraction in the development of Mobius syndrome. J Child Neurol 1997;12:225-227.
-
(1997)
J Child Neurol
, vol.12
, pp. 225-227
-
-
Graf, W.D.1
Shepard, T.H.2
-
15
-
-
0025122294
-
Moebius syndrome
-
Kumar D. Moebius syndrome. J Med Genet 1990;27:122-126.
-
(1990)
J Med Genet
, vol.27
, pp. 122-126
-
-
Kumar, D.1
-
16
-
-
0030789806
-
Is there a zone of vascular vulnerability in the fetal brain stem?
-
Leong S, Ashwell KW. Is there a zone of vascular vulnerability in the fetal brain stem? Neurotoxicol Teratol 1997;19:265-275.
-
(1997)
Neurotoxicol Teratol
, vol.19
, pp. 265-275
-
-
Leong, S.1
Ashwell, K.W.2
-
18
-
-
0025884458
-
Deletion of chromosome 13 in Moebius syndrome
-
Slee JJ, Smart RD, Viljoen DL. Deletion of chromosome 13 in Moebius 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
Viljoen, D.L.3
-
19
-
-
0017626152
-
Three generation pedigree of a Mobius syndrome variant with chromosome translocation
-
Ziter FA, Wiser WC, Robinson A. Three generation pedigree of a Mobius syndrome variant with chromosome translocation. Arch Neurol 1977;34:437-442.
-
(1977)
Arch Neurol
, vol.34
, pp. 437-442
-
-
Ziter, F.A.1
Wiser, W.C.2
Robinson, A.3
-
20
-
-
0030610414
-
Mobius-like syndrome associated with a 1;2 chromosome translocation
-
Nishikawa M, Ichiyama T, Hayashi T, Furukawa S. Mobius-like syndrome associated with a 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
Furukawa, S.4
-
21
-
-
0034106877
-
Prefrontal and medial temporal correlates of repetitive violence to self and others
-
Critchley HD, Simmon A, Daly EM, Russell A, van Amelsvoort Teck, Robertson DM, et al. Prefrontal and medial temporal correlates of repetitive violence to self and others. Biol Psychiatry 2000;47:928-934.
-
(2000)
Biol Psychiatry
, vol.47
, pp. 928-934
-
-
Critchley, H.D.1
Simmon, A.2
Daly, E.M.3
Russell, A.4
Van Amelsvoort, T.5
Robertson, D.M.6
-
22
-
-
0035374905
-
The impact of childhood abuse and neglect on adult mental health: A prospective study
-
Horowitz AV, Widom CS, McLaughlin J, White HR. The impact of childhood abuse and neglect on adult mental health: a prospective study. J Health Soc Behav 2001;42:184-201.
-
(2001)
J Health Soc Behav
, vol.42
, pp. 184-201
-
-
Horowitz, A.V.1
Widom, C.S.2
McLaughlin, J.3
White, H.R.4
-
23
-
-
0033964920
-
Reduced prefrontal gray matter volume and reduced autonomic activity in antisocial personality disorder
-
Raine A, Lencz T, Bihrle S, LaCasse L, Colletti P. Reduced prefrontal gray matter volume and reduced autonomic activity in antisocial personality disorder. Arch Gen Psychiatry 2000;57:119-127.
-
(2000)
Arch Gen Psychiatry
, vol.57
, pp. 119-127
-
-
Raine, A.1
Lencz, T.2
Bihrle, S.3
LaCasse, L.4
Colletti, P.5
-
24
-
-
0032496293
-
Behavioral phenotypes: Conceptual and methodological issues
-
Flint J. Behavioral phenotypes: conceptual and methodological issues. Am J Med Genet 1998;81:235-240.
-
(1998)
Am J Med Genet
, vol.81
, pp. 235-240
-
-
Flint, J.1
-
25
-
-
0027442475
-
Abnormal behavior associated with a point mutation in the structural gene for monoamine oxidase A
-
Brunner HG, Nelen M, Breakefield XO, Ropers HH, Van Ost BA. Abnormal behavior associated with a point mutation in the structural gene for monoamine oxidase A. Science 1993;262:578-580.
-
(1993)
Science
, vol.262
, pp. 578-580
-
-
Brunner, H.G.1
Nelen, M.2
Breakefield, X.O.3
Ropers, H.H.4
Van Ost, B.A.5
-
26
-
-
0028845340
-
Behavioral abnormalities in male mice lacking neuronal nitric oxide synthase
-
Nelson RJ, Demas GE, Huang PL, Fishman MC, Dawson VL, Dawson TM, et al. Behavioral abnormalities in male mice lacking neuronal nitric oxide synthase. Nature 1995;378:383-386.
-
(1995)
Nature
, vol.378
, pp. 383-386
-
-
Nelson, R.J.1
Demas, G.E.2
Huang, P.L.3
Fishman, M.C.4
Dawson, V.L.5
Dawson, T.M.6
-
29
-
-
0026033949
-
Assignment of a serotonin 5HT-2 receptor gene (5HTR2) to human chromosome 13q14-21 and mouse chromosome 14
-
Sparkes RS, Lan N, Klisak I, Mohandas T, Diep A, Kojis T, et al. Assignment of a serotonin 5HT-2 receptor gene (5HTR2) to human chromosome 13q14-21 and mouse chromosome 14. Genomics 1991;9:461-465.
-
(1991)
Genomics
, vol.9
, pp. 461-465
-
-
Sparkes, R.S.1
Lan, N.2
Klisak, I.3
Mohandas, T.4
Diep, A.5
Kojis, T.6
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