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I Feenstra

Showing results (11-20 of 12) with videos related to

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Clinical Genetics|April 6, 2013
Novel BCOR mutations in patients with oculofaciocardiodental (OFCD) syndromeH E Feberwee, I Feenstra, S Oberoi, et al.
Clinical Genetics|April 21, 2018
Further audiovestibular characterization of DFNB77, caused by deleterious variants in LOXHD1, and investigation into the involvement of Fuchs corneal dystrophyM Wesdorp, V Schreur, A J Beynon, et al.
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Showing results (11-20 of 12) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 12 results.
Clinical Genetics|April 6, 2013
Novel BCOR mutations in patients with oculofaciocardiodental (OFCD) syndromeH E Feberwee, I Feenstra, S Oberoi, et al.
Clinical Genetics|April 21, 2018
Further audiovestibular characterization of DFNB77, caused by deleterious variants in LOXHD1, and investigation into the involvement of Fuchs corneal dystrophyM Wesdorp, V Schreur, A J Beynon, et al.
Pageof 2