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1992 | 1 |
1997 | 1 |
2024 | 0 |
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Causal heterogeneity in isolated lissencephaly.
Neurology. 1992 Jul;42(7):1375-88. doi: 10.1212/wnl.42.7.1375.
Neurology. 1992.
PMID: 1620349
Dominant X linked subcortical laminar heterotopia and lissencephaly syndrome (XSCLH/LIS): evidence for the occurrence of mutation in males and mapping of a potential locus in Xq22.
des Portes V, Pinard JM, Smadja D, Motte J, Boespflüg-Tanguy O, Moutard ML, Desguerre I, Billuart P, Carrie A, Bienvenu T, Vinet MC, Bachner L, Beldjord C, Dulac O, Kahn A, Ponsot G, Chelly J.
des Portes V, et al.
J Med Genet. 1997 Mar;34(3):177-83. doi: 10.1136/jmg.34.3.177.
J Med Genet. 1997.
PMID: 9132485
Free PMC article.
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