Jennifer N Dines

1PUBLICATIONS
1CO-AUTHORS
Developmental genetics (incl. sex determination)
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Publications (1)

|Jul 12, 2019
Expanding phenotype with severe midline brain anomalies and missense variant supports a causal role for FOXA2 in 20p11.2 deletion syndrome.

Jennifer N Dines, Yajuan J Liu, Whitney Neufeld-Kaiser

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Frequent Collaborators

1 joint publications

Yajuan J Liu