Pages that link to "Q57905599"
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The following pages link to Investigation of the 15q13.3 CNV as a genetic modifier for familial epilepsies with variable phenotypes (Q57905599):
Displaying 5 items.
- Investigation of 15q11-q13, 16p11.2 and 22q13 CNVs in autism spectrum disorder Brazilian individuals with and without epilepsy (Q34257185) (← links)
- Where genotype is not predictive of phenotype: towards an understanding of the molecular basis of reduced penetrance in human inherited disease (Q37187461) (← links)
- Association study of the 2-bp deletion polymorphism in exon 6 of the CHRFAM7A gene with idiopathic generalized epilepsy. (Q37250558) (← links)
- The role of T-type calcium channel genes in absence seizures (Q38213389) (← links)
- Rare exonic deletions of the RBFOX1 gene increase risk of idiopathic generalized epilepsy (Q46499520) (← links)