-
1
-
-
7844223263
-
LIS1 and XLIS (DCX) mutations cause most classical lissencephaly, but different patterns of malformation
-
Pilz DT, Matsumoto N, Minnerath S, et al. LIS1 and XLIS (DCX) mutations cause most classical lissencephaly, but different patterns of malformation. Hum Mol Genet 1998;7:2029-2037
-
(1998)
Hum Mol Genet
, vol.7
, pp. 2029-2037
-
-
Pilz, D.T.1
Matsumoto, N.2
Minnerath, S.3
-
3
-
-
0029000061
-
Lissencephaly and other malformations of cortical development: 1995 update
-
Dobyns WB, Truwit CL. Lissencephaly and other malformations of cortical development: 1995 update. Neuropediatrics 1995;26:132-147
-
(1995)
Neuropediatrics
, vol.26
, pp. 132-147
-
-
Dobyns, W.B.1
Truwit, C.L.2
-
4
-
-
0029804898
-
Lissencephaly with extreme cerebral and cerebellar hypoplasia: A magnetic resonance imaging study
-
Kroon AA, Smit BJ, Barth PG, Hennekam RC. Lissencephaly with extreme cerebral and cerebellar hypoplasia: a magnetic resonance imaging study. Neuropediatrics 1996;27:273-276
-
(1996)
Neuropediatrics
, vol.27
, pp. 273-276
-
-
Kroon, A.A.1
Smit, B.J.2
Barth, P.G.3
Hennekam, R.C.4
-
5
-
-
0030959134
-
Lissencephaly associated with cerebellar hypoplasia and myoclonic epilepsy in a Bedouin kindred: A new syndrome?
-
Farah S, Sabry MA, Khuraibet A, et al. Lissencephaly associated with cerebellar hypoplasia and myoclonic epilepsy in a Bedouin kindred: a new syndrome? Clin Genet 1997;51: 326-330
-
(1997)
Clin Genet
, vol.51
, pp. 326-330
-
-
Farah, S.1
Sabry, M.A.2
Khuraibet, A.3
-
8
-
-
0028859547
-
Two cases of possible cerebrocerebellar lissencephaly variant of type I
-
Sugama S, Kusano K. Two cases of possible cerebrocerebellar lissencephaly variant of type I [Japanese]. No Hattatsu 1995; 27:502-504
-
(1995)
No Hattatsu
, vol.27
, pp. 502-504
-
-
Sugama, S.1
Kusano, K.2
-
9
-
-
0024254187
-
Cerebellar agenesia associated with microcephaly and agyria: Report of a case in a newborn and review of the literature
-
Pittella JE, Nogueira AM. Cerebellar agenesia associated with microcephaly and agyria: report of a case in a newborn and review of the literature [Portugese]. Arq Neuro-Psiquiat 1988; 46:385-392
-
(1988)
Arq Neuro-Psiquiat
, vol.46
, pp. 385-392
-
-
Pittella, J.E.1
Nogueira, A.M.2
-
10
-
-
0027200304
-
A sibship with a neuronal migration defect, cerebellar hypoplasia and congenital lymphedema
-
Hourihane JO, Bennett CP, Chaudhuri R, et al. A sibship with a neuronal migration defect, cerebellar hypoplasia and congenital lymphedema. Neuropediatrics 1993;24:43-46
-
(1993)
Neuropediatrics
, vol.24
, pp. 43-46
-
-
Hourihane, J.O.1
Bennett, C.P.2
Chaudhuri, R.3
-
11
-
-
0344423452
-
Cerebro-cerebellar lissencephaly, congenital heart defects and other congenital anomalies in male sibs: A new syndrome
-
Vancouver, BC, Canada
-
McComb R, Schaefer B, Olney A, Hattie B. Cerebro-cerebellar lissencephaly, congenital heart defects and other congenital anomalies in male sibs: a new syndrome. Presented at the 23rd Annual March of Dimes Clinical Genetics Conference on Developmental and Genetic Disorders of the Central Nervous System, Vancouver, BC, Canada, 1991
-
(1991)
23rd Annual March of Dimes Clinical Genetics Conference on Developmental and Genetic Disorders of the Central Nervous System
-
-
McComb, R.1
Schaefer, B.2
Olney, A.3
Hattie, B.4
|