Rachel A Veazey

1PUBLICATIONS
2CO-AUTHORS
Developmental genetics (incl. sex determination)
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Publications (1)

|Oct 10, 2024
Novel Missense Variant in the SMARCD1 Gene as the Cause of Coffin-Siris Syndrome 11 in a Fetus With Ambiguous Genitalia and Multiple Dysmorphic Features.

Rachel A Veazey, Allan J Fisher, Asha N Talati

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Frequent Collaborators

1 joint publications

Asha N Talati

1 joint publications

Neeta L Vora