Home
About
Overview
Sharing Data
ORCID
Help
History (0)
Find People
Find Everything
Login
to edit your profile (add a photo, awards, links to other websites, etc.)
Edit My Profile
My Person List (
0
)
Return to Top
Search Result Details
Back to Search Results
This page shows the details of why an item matched the keywords from your search.
Search Results
Rasmussen, Astrid
One or more keywords matched the following items that are connected to
Rasmussen, Astrid
Item Type
Name
Concept
DNA Mutational Analysis
Academic Article
Clinical heterogeneity of recessive ataxia in the Mexican population.
Academic Article
DNA variants in coding region of EFHC1: SNPs do not associate with juvenile myoclonic epilepsy.
Academic Article
Von Hippel-Lindau disease germline mutations in Mexican patients with cerebellar hemangioblastoma.
Academic Article
Founder effect for the Ala431Glu mutation of the presenilin 1 gene causing early-onset Alzheimer's disease in Mexican families.
Academic Article
Identification and mutational analysis of candidate genes for juvenile myoclonic epilepsy on 6p11-p12: LRRC1, GCLC, KIAA0057 and CLIC5.
Academic Article
Presymptomatic diagnosis in Huntington's disease: the Mexican experience.
Search Criteria
DNA Mutational Analysis