Kristin D Kernohan

2PUBLICATIONS
3CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Cell and nuclear division
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Publications (2)

|Jan 18, 2024
The expanding diagnostic toolbox for rare genetic diseases.

Kristin D Kernohan, Kym M Boycott

|Dec 05, 2023
RNA sequencing reveals deep intronic CEP120 variant: A report of the diagnostic odyssey for two siblings with Joubert syndrome type 31.

Aren E Marshall, Gabrielle Lemire, Yijing Liang

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