Sentence examples for forms of lis from inspiring English sources

Mutations in several other genes including ARX, RELN and VLDLR have been identified in other forms of LIS but collectively these account for only a small proportion of patients with LIS.

Some rare forms of LIS are associated with a disproportionately small cerebellum, referred to as lissencephaly with cerebellar hypoplasia (LCH).

However, some rare forms of LIS are associated with a disproportionately small cerebellum, referred to as LIS with cerebellar hypoplasia (LCH).

In the most severe form, the surface of the cerebral hemispheres is completely smooth (agyria), whereas less severe forms of LIS are characterized by simplified folding patterns with abnormally broad gyri (pachygyria).

We immediately recognized that mutations involving the arginine residue at codon 402 resulted in phenotypes indistinguishable from those associated with mutations of the LIS1 gene, while mutations at other codons produced more complex forms of LIS.

We previously showed that mutations in LIS1 and DCX account for ∼85% of patients with the classic form of lissencephaly (LIS).

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In addition, it can be seen that the structural parameters mainly influenced the insulation performance of LIS by changing the areal density of LIS.

However, predictive validity of both scores was marginal, and there was no additive value of LIS over Berlin.

Our data predict that another ∼1% of patients with classic LIS will have mutations of TUBA1A (i.e. 7% of the remaining 15% of LIS yet unexplained).