-
1
-
-
0028954840
-
A frameshift mutation in the gene for PAX3 in a girl with spina bifida and mud signs of Waardenburg syndrome
-
Hol F, Hamel B, Geurds M, Mullaart R, Barr F, Marina R, Mariman E: A frameshift mutation in the gene for PAX3 in a girl with spina bifida and mud signs of Waardenburg syndrome. J Med Genet 32 (1995) 52-56
-
(1995)
J Med Genet
, vol.32
, pp. 52-56
-
-
Hol, F.1
Hamel, B.2
Geurds, M.3
Mullaart, R.4
Barr, F.5
Marina, R.6
Mariman, E.7
-
2
-
-
4243459140
-
Molecular genetics of hydrocephalus - Fine structural mapping of the congenital hydrocephalns (ch) mouse mutant
-
Hong H, Chakravarti A. Molecular genetics of hydrocephalus - Fine structural mapping of the congenital hydrocephalns (ch) mouse mutant Am J Hum Genet 57 (4 SS) (1995) 756
-
(1995)
Am J Hum Genet
, vol.57
, Issue.4 SS
, pp. 756
-
-
Hong, H.1
Chakravarti, A.2
-
3
-
-
0023113381
-
Morphological aspects of the development of hydrocephalus in a mouse mutant (SUMS/NP)
-
Jones H, Dack S, Ellis C: Morphological aspects of the development of hydrocephalus in a mouse mutant (SUMS/NP). Acta Neuropathol (Berl) 72 (1987) 268-276
-
(1987)
Acta Neuropathol (Berl)
, vol.72
, pp. 268-276
-
-
Jones, H.1
Dack, S.2
Ellis, C.3
-
4
-
-
0030029134
-
X-linked hydrocephalus and MASA syndrome
-
Kenwrick S, Jouet M, Donnai D: X-linked hydrocephalus and MASA syndrome. J Med Genet 33 (1996) 59-65
-
(1996)
J Med Genet
, vol.33
, pp. 59-65
-
-
Kenwrick, S.1
Jouet, M.2
Donnai, D.3
-
5
-
-
0019427490
-
A new model of congenital hydrocephalus in the rat
-
Kohn D, Chinookoswong N, Chou S: A new model of congenital hydrocephalus in the rat. Acta Neuropathol 54 (1981) 211-218
-
(1981)
Acta Neuropathol
, vol.54
, pp. 211-218
-
-
Kohn, D.1
Chinookoswong, N.2
Chou, S.3
-
6
-
-
0022312729
-
Congenital genetic murine (ch) hydrocephalus
-
Richardson R: Congenital genetic murine (ch) hydrocephalus. Child's Nerv Syst 1 (1985) 87-99
-
(1985)
Child's Nerv Syst
, vol.1
, pp. 87-99
-
-
Richardson, R.1
-
7
-
-
84970061068
-
Aberrant splicing of neural cell adhesion molecule L1 mRNA in a family with X-linked hydrocephalus
-
Rosenthal A, Jouet M, Kenwrick S: Aberrant splicing of neural cell adhesion molecule L1 mRNA in a family with X-linked hydrocephalus. Nature Genet 2 (1992) 107-112
-
(1992)
Nature Genet
, vol.2
, pp. 107-112
-
-
Rosenthal, A.1
Jouet, M.2
Kenwrick, S.3
-
8
-
-
0021055872
-
Congenital hydrocephalus revealed in the inbred rat, LEW/jms
-
Sasaki S, Goto H, Nagano H, Furuya K, Omata Y, Kanazawa K, Suzuki K, Sudo K, Collmann H: Congenital hydrocephalus revealed in the inbred rat, LEW/jms. Neurosurgery 13 (1983) 548-554
-
(1983)
Neurosurgery
, vol.13
, pp. 548-554
-
-
Sasaki, S.1
Goto, H.2
Nagano, H.3
Furuya, K.4
Omata, Y.5
Kanazawa, K.6
Suzuki, K.7
Sudo, K.8
Collmann, H.9
-
9
-
-
0029932086
-
Transcription factor AP-2 essential for cranial closure and cramofacial development
-
Schorle H, Meier P, Buchert M, Jaenisch R, Mitchell P: Transcription factor AP-2 essential for cranial closure and cramofacial development Nature 381 (1996) 235-238
-
(1996)
Nature
, vol.381
, pp. 235-238
-
-
Schorle, H.1
Meier, P.2
Buchert, M.3
Jaenisch, R.4
Mitchell, P.5
-
10
-
-
0028844492
-
Mutated methylenetetrahydrofolate reductase as a risk factor for spina bifida
-
van der Put N, Steegers-Theunissen R, Frosst P, Trijbels F, Eskes T, van der Heuvel L, Mariman E, den Heyer M, Rozen R, Blom H: Mutated methylenetetrahydrofolate reductase as a risk factor for spina bifida. Lancet 346 (1995) 1070-1071
-
(1995)
Lancet
, vol.346
, pp. 1070-1071
-
-
Van der Put, N.1
Steegers-Theunissen, R.2
Frosst, P.3
Trijbels, F.4
Eskes, T.5
Van der Heuvel, L.6
Mariman, E.7
Den Heyer, M.8
Rozen, R.9
Blom, H.10
-
11
-
-
0030034268
-
Relevance to spina bifida of mutated methylenetetrahydrofolate reductase
-
Wilcken D, Wang X: Relevance to spina bifida of mutated methylenetetrahydrofolate reductase. Lancet 347 (1996) 340
-
(1996)
Lancet
, vol.347
, pp. 340
-
-
Wilcken, D.1
Wang, X.2
-
12
-
-
0029932525
-
Neural tube, skeletal and body wall defects in mice lacking transcription factor AP-2
-
Zhang J, Hagopian-Donaldson S, Serbedzija G, Elsemore J, Plehn-Dujowich D, McMahon A, Flavell R, Williams T: Neural tube, skeletal and body wall defects in mice lacking transcription factor AP-2 Nature 381 (1996) 238-241
-
(1996)
Nature
, vol.381
, pp. 238-241
-
-
Zhang, J.1
Hagopian-Donaldson, S.2
Serbedzija, G.3
Elsemore, J.4
Plehn-Dujowich, D.5
McMahon, A.6
Flavell, R.7
Williams, T.8
-
13
-
-
0028040327
-
Familial hydrocephalus of prenatal onset
-
Zlotogora J, Sagi M, Cohen T: Familial hydrocephalus of prenatal onset Am J Med Genet 49 (1994) 202-204
-
(1994)
Am J Med Genet
, vol.49
, pp. 202-204
-
-
Zlotogora, J.1
Sagi, M.2
Cohen, T.3
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