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Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

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Debbie S Kuo

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Human Molecular Genetics|November 9, 2013

Allelic heterogeneity contributes to variability in ocular dysgenesis, myopathy and brain malformations caused by Col4a1 and Col4a2 mutationsDebbie S Kuo, Cassandre Labelle-Dumais, Mao Mao, et al.

Plos One|August 23, 2017

Characterization of a variant of gap junction protein α8 identified in a family with hereditary cataractDebbie S Kuo, Jared T Sokol, Peter J Minogue, et al.

European Journal of Human Genetics : EJHG|February 16, 2012

COL4A2 mutation associated with familial porencephaly and small-vessel diseaseElly Verbeek, Marije E C Meuwissen, Frans W Verheijen, et al.

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Search research articles

Showing results (11-20 of 13) with videos related to

Sort By:

Pageof 2

You have reached the last page of results.This site can display upto 13 results.

Human Molecular Genetics|November 9, 2013

Allelic heterogeneity contributes to variability in ocular dysgenesis, myopathy and brain malformations caused by Col4a1 and Col4a2 mutationsDebbie S Kuo, Cassandre Labelle-Dumais, Mao Mao, et al.

Plos One|August 23, 2017

Characterization of a variant of gap junction protein α8 identified in a family with hereditary cataractDebbie S Kuo, Jared T Sokol, Peter J Minogue, et al.

European Journal of Human Genetics : EJHG|February 16, 2012

COL4A2 mutation associated with familial porencephaly and small-vessel diseaseElly Verbeek, Marije E C Meuwissen, Frans W Verheijen, et al.

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