Astrid Rasmussen to DNA Mutational Analysis
This is a "connection" page, showing publications Astrid Rasmussen has written about DNA Mutational Analysis.
Connection Strength
0.256
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Presymptomatic diagnosis in Huntington's disease: the Mexican experience. Genet Test Mol Biomarkers. 2009 Dec; 13(6):717-20.
Score: 0.081
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Clinical heterogeneity of recessive ataxia in the Mexican population. J Neurol Neurosurg Psychiatry. 2006 Dec; 77(12):1370-2.
Score: 0.066
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Von Hippel-Lindau disease germline mutations in Mexican patients with cerebellar hemangioblastoma. J Neurosurg. 2006 Mar; 104(3):389-94.
Score: 0.062
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DNA variants in coding region of EFHC1: SNPs do not associate with juvenile myoclonic epilepsy. Epilepsia. 2009 May; 50(5):1184-90.
Score: 0.019
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Founder effect for the Ala431Glu mutation of the presenilin 1 gene causing early-onset Alzheimer's disease in Mexican families. Neurogenetics. 2006 Jul; 7(3):195-200.
Score: 0.016
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Identification and mutational analysis of candidate genes for juvenile myoclonic epilepsy on 6p11-p12: LRRC1, GCLC, KIAA0057 and CLIC5. Epilepsy Res. 2002 Aug; 50(3):265-75.
Score: 0.012