Differences in the gyral pattern distinguish chromosome 17–linked and X-linked lissencephaly

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Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

1. 1LIS1 and XLIS (DCX) mutations cause most classical lissencephaly, but different patterns of malformation1998 · 354 citations
2. 2Fluorescence in situ hybridization analysis with LIS1 specific probes reveals a high deletion mutation rate in isolated lissencephaly sequence1998 · 53 citations
3. 3Human doublecortin (DCX) and the homologous gene in mouse encode a putative Ca2+-dependent signaling protein which is mutated in human X- linked neuronal migration defects1998 · 96 citations
4. 4A Revision of the Lissencephaly and Miller-Dieker Syndrome Critical Regions in Chromosome 17p13.31997 · 192 citations
5. 5Characterization of mutations in the genedoublecortin in patients with double cortex syndrome1999 · 166 citations