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.

MLA

des Portes, V., et al. “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.” Journal of Medical Genetics, vol. 34, no. 3, Mar. 1997, pp. 177–83. EBSCOhost, https://doi.org/10.1136/jmg.34.3.177.

APA

des Portes, V., Pinard, J. M., Smadja, D., Motte, J., Boespflüg-Tanguy, O., Moutard, M. L., Desguerre, I., Billuart, P., Carrie, A., Bienvenu, T., Vinet, M. C., Bachner, L., Beldjord, C., Dulac, O., Kahn, A., Ponsot, G., & Chelly, J. (1997). 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. Journal of Medical Genetics, 34(3), 177–183. https://doi.org/10.1136/jmg.34.3.177

Chicago

des Portes, V, J M Pinard, D Smadja, J Motte, O Boespflüg-Tanguy, M L Moutard, I Desguerre, et al. 1997. “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.” Journal of Medical Genetics 34 (3): 177–83. doi:10.1136/jmg.34.3.177.