Wai-Man Chan
3PUBLICATIONS
48CO-AUTHORS
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Publications (3)
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|Sep 27, 2024
A cell type-aware framework for nominating non-coding variants in Mendelian regulatory disorders.Arthur S Lee, Lauren J Ayers, Michael Kosicki
|Jun 29, 2023
Noncoding variants alter GATA2 expression in rhombomere 4 motor neurons and cause dominant hereditary congenital facial paresis.Alan P Tenney, Silvio Alessandro Di Gioia, Bryn D Webb
|Oct 15, 2021
TUBB3 Arg262His causes a recognizable syndrome including CFEOM3, facial palsy, joint contractures, and early-onset peripheral neuropathy.Mary C Whitman, Brenda J Barry, Caroline D Robson
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Elizabeth C Engle
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Mary C Whitman
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Caroline D Robson
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Monkol Lek
2 joint publications
Len A Pennacchio
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Irini Manoli
2 joint publications
Ethylin Wang Jabs
1 joint publications
Michael E Talkowski
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Tanya J Lehky
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Audrey Thurm
