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Year | Number of Results |
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2007 | 1 |
2012 | 1 |
2016 | 1 |
2024 | 0 |
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Page 1
Molecular heterogeneity in fetal forms of type II lissencephaly.
Hum Mutat. 2007 Oct;28(10):1020-7. doi: 10.1002/humu.20561.
Hum Mutat. 2007.
PMID: 17559086
Cobblestone lissencephaly: neuropathological subtypes and correlations with genes of dystroglycanopathies.
Devisme L, Bouchet C, Gonzalès M, Alanio E, Bazin A, Bessières B, Bigi N, Blanchet P, Bonneau D, Bonnières M, Bucourt M, Carles D, Clarisse B, Delahaye S, Fallet-Bianco C, Figarella-Branger D, Gaillard D, Gasser B, Delezoide AL, Guimiot F, Joubert M, Laurent N, Laquerrière A, Liprandi A, Loget P, Marcorelles P, Martinovic J, Menez F, Patrier S, Pelluard F, Perez MJ, Rouleau C, Triau S, Attié-Bitach T, Vuillaumier-Barrot S, Seta N, Encha-Razavi F.
Devisme L, et al.
Brain. 2012 Feb;135(Pt 2):469-82. doi: 10.1093/brain/awr357. Epub 2012 Feb 9.
Brain. 2012.
PMID: 22323514
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Analysis of phenotype, enzyme activity and genotype of Chinese patients with POMT1 mutation.
Yang H, Manya H, Kobayashi K, Jiao H, Fu X, Xiao J, Li X, Wang J, Jiang Y, Toda T, Endo T, Wu X, Xiong H.
Yang H, et al.
J Hum Genet. 2016 Aug;61(8):753-9. doi: 10.1038/jhg.2016.42. Epub 2016 May 19.
J Hum Genet. 2016.
PMID: 27193224
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