Résultats de la recherche

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(1 - 8 of 8)
A novel recurrent LIS1 splice site mutation in classic lissencephaly
Rare ACTG1 variants in fetal microlissencephaly
ARX polyalanine expansions are highly implicated in familial cases of mental retardation with infantile epilepsy and/or hand dystonia
Characterization of human disease phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1

Islandora displays