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Clinical Genetics|May 23, 2009
Four novel SPG3A/atlastin mutations identified in autosomal dominant hereditary spastic paraplegia kindreds with intra-familial variability in age of onset and complex phenotypeB N Smith, S Bevan, C Vance, et al.
Human Reproduction Update|February 21, 2012
The ESHRE PGD Consortium: 10 years of data collectionJ C Harper, L Wilton, J Traeger-Synodinos, et al.
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Showing results (21-30 of 22) with videos related to

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Pageof 3
You have reached the last page of results.This site can display upto 22 results.
Clinical Genetics|May 23, 2009
Four novel SPG3A/atlastin mutations identified in autosomal dominant hereditary spastic paraplegia kindreds with intra-familial variability in age of onset and complex phenotypeB N Smith, S Bevan, C Vance, et al.
Human Reproduction Update|February 21, 2012
The ESHRE PGD Consortium: 10 years of data collectionJ C Harper, L Wilton, J Traeger-Synodinos, et al.
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