Carly Smith

5PUBLICATIONS
2CO-AUTHORS
Foetal development and medicineGene expression (incl. microarray and other genome-wide approaches)Epigenetics (incl. genome methylation and epigenomics)
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Publications (5)

|May 23, 2026
Hereditary Spherocytosis: A Case Series Spanning Prenatal Detection to Neonatal Care.

|Jul 09, 2024
Fetal phenotype and diagnosis of autosomal dominant Robinow syndrome due to novel DVL1 variant.

Carly M Smith, Kristi Guinon, Suha Bachir

|Jan 01, 2024
Raine syndrome: Prenatally identified severe craniofacial phenotype with multisuture synostosis and brain abnormalities associated with variants in FAM20C.

Courtney P Verscaj, Carly Smith, Margaret Homeyer

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Frequent Collaborators

1 joint publications

Gabrielle R Barsh

1 joint publications

Courtney P Verscaj