-
1
-
-
0032422555
-
Mutations in filamin 1 prevent migration of cerebral cortical neurons in human periventricular heterotopia
-
Fox JW, Lamperti ED, Eksioglu YZ, et al. Mutations in filamin 1 prevent migration of cerebral cortical neurons in human periventricular heterotopia. Neuron 1998;21:1315-1325.
-
(1998)
Neuron
, vol.21
, pp. 1315-1325
-
-
Fox, J.W.1
Lamperti, E.D.2
Eksioglu, Y.Z.3
-
2
-
-
0035880455
-
Mutations in the X-linked filamin 1 gene cause periventricular nodular heterotopia in males as well as in females
-
Sheen VL, Dixon PH, Fox JW, et al. Mutations in the X-linked filamin 1 gene cause periventricular nodular heterotopia in males as well as in females. Hum Mol Genet 2001;10:1775-1783.
-
(2001)
Hum Mol Genet
, vol.10
, pp. 1775-1783
-
-
Sheen, V.L.1
Dixon, P.H.2
Fox, J.W.3
-
3
-
-
0037177085
-
Familial periventricular heterotopia: Missense and distal truncating mutations of the FLN1 gene
-
Moro F, Carrozzo R, Veggiotti P, et al. Familial periventricular heterotopia: missense and distal truncating mutations of the FLN1 gene. Neurology 2002;58:916-921.
-
(2002)
Neurology
, vol.58
, pp. 916-921
-
-
Moro, F.1
Carrozzo, R.2
Veggiotti, P.3
-
5
-
-
0029927897
-
Ehlers-Danlos syndrome with subependymal periventricular heterotopias
-
Thomas P, Bossan A, Lacour JP, Chanalet S, Ortonne JP, Chatel M. Ehlers-Danlos syndrome with subependymal periventricular heterotopias. Neurology 1996;46:1165-1167.
-
(1996)
Neurology
, vol.46
, pp. 1165-1167
-
-
Thomas, P.1
Bossan, A.2
Lacour, J.P.3
Chanalet, S.4
Ortonne, J.P.5
Chatel, M.6
-
6
-
-
0033736569
-
Periventricular nodular heterotopia in patients with filamin-1 gene mutations: Neuroimaging findings
-
Poussaint TY, Fox JW, Dobyns WB, et al. Periventricular nodular heterotopia in patients with filamin-1 gene mutations: neuroimaging findings. Pediatr Radiol 2000;30:748-755.
-
(2000)
Pediatr Radiol
, vol.30
, pp. 748-755
-
-
Poussaint, T.Y.1
Fox, J.W.2
Dobyns, W.B.3
-
7
-
-
0036556466
-
Identification of a dup(5)(p15.3) by multicolor banding
-
Riordan D, Vust A, Wickstrom D, et al. Identification of a dup(5)(p15.3) by multicolor banding. Clin Genet 2002;61:277-282.
-
(2002)
Clin Genet
, vol.61
, pp. 277-282
-
-
Riordan, D.1
Vust, A.2
Wickstrom, D.3
-
8
-
-
0037105012
-
De novo complete trisomy 5p: Clinical and neuroradiological findings
-
Grosso S, Cioni M, Garibaldi G, et al. De novo complete trisomy 5p: clinical and neuroradiological findings. Am J Med Genet 2002;112:56-60.
-
(2002)
Am J Med Genet
, vol.112
, pp. 56-60
-
-
Grosso, S.1
Cioni, M.2
Garibaldi, G.3
-
9
-
-
0032169814
-
Partial tetrasomy with triplication of chromosome (5) (p14-p15.33) in a patient with severe multiple congenital anomalies
-
Harrison KJ, Teshima IE, Silver MM, et al. Partial tetrasomy with triplication of chromosome (5) (p14-p15.33) in a patient with severe multiple congenital anomalies. Am J Med Genet 1998;79:103-107.
-
(1998)
Am J Med Genet
, vol.79
, pp. 103-107
-
-
Harrison, K.J.1
Teshima, I.E.2
Silver, M.M.3
-
10
-
-
0034844532
-
Beyond the Hox: How widespread is homeobox gene clustering?
-
Holland PW. Beyond the Hox: how widespread is homeobox gene clustering? J Anat 2001;199(pt 1-2):13-23.
-
(2001)
J Anat
, vol.199
, Issue.PART 1-2
, pp. 13-23
-
-
Holland, P.W.1
|