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Journal of Neurology
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July 5, 2001
Mutation analysis in Chariot-Marie Tooth disease type 1: point mutations in the MPZ gene and the GJB1 gene cause comparable phenotypic heterogeneity
P Young, K Grote, G Kuhlenbäumer, et al.
Pediatrics
|
June 1, 1997
Lipoprotein (a): its role in childhood thromboembolism
U Nowak-Göttl, O Debus, M Findeisen, et al.
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of 2
Search research articles
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Showing results (11-20 of 12) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 12 results.
Journal of Neurology
|
July 5, 2001
Mutation analysis in Chariot-Marie Tooth disease type 1: point mutations in the MPZ gene and the GJB1 gene cause comparable phenotypic heterogeneity
P Young, K Grote, G Kuhlenbäumer, et al.
Pediatrics
|
June 1, 1997
Lipoprotein (a): its role in childhood thromboembolism
U Nowak-Göttl, O Debus, M Findeisen, et al.
Page
of 2