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Clinical Genetics
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May 29, 2010
C2orf37 mutational spectrum in Woodhouse-Sakati syndrome patients
A M Alazami, S A Schneider, D Bonneau, et al.
Human Molecular Genetics
|
April 3, 2023
Pathogenic SCN2A variants cause early-stage dysfunction in patient-derived neurons
R Asadollahi, I Delvendahl, R Muff, et al.
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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.
Clinical Genetics
|
May 29, 2010
C2orf37 mutational spectrum in Woodhouse-Sakati syndrome patients
A M Alazami, S A Schneider, D Bonneau, et al.
Human Molecular Genetics
|
April 3, 2023
Pathogenic SCN2A variants cause early-stage dysfunction in patient-derived neurons
R Asadollahi, I Delvendahl, R Muff, et al.
Page
of 2