Carly M Smith (Carly Smith)

Publication Activity (10 Years)

Years Active: 2024-2024
Publications (10 Years): 9

Top Topics

Preterm Infants

Contrast Enhanced Ultrasound

Duchenne Muscular Dystrophy

Top Venues

Prenatal diagnosis

This page only lists publications with an associated author ORCID identifier.

Publications

Carly M Smith, Kristi Guinon, Suha Bachir, Christina G Tise
Fetal phenotype and diagnosis of autosomal dominant Robinow syndrome due to novel DVL1 variant. Prenatal diagnosis 44 (9) (2024)
Courtney P Verscaj, Carly M Smith, Margaret Homeyer, Dena R Matalon
Raine syndrome: Prenatally identified severe craniofacial phenotype with multisuture synostosis and brain abnormalities associated with variants in FAM20C. Prenatal diagnosis 44 (3) (2024)
Courtney P Verscaj, Carly M Smith, Margaret Homeyer, Dena R Matalon
Raine syndrome: Prenatally identified severe craniofacial phenotype with multisuture synostosis and brain abnormalities associated with variants in FAM20C. Prenatal diagnosis 44 (3) (2024)
Carly M Smith, Kristi Guinon, Suha Bachir, Christina G Tise
Fetal phenotype and diagnosis of autosomal dominant Robinow syndrome due to novel DVL1 variant. Prenatal diagnosis 44 (9) (2024)
Carly M Smith, Kristi Guinon, Suha Bachir, Christina G Tise
Fetal phenotype and diagnosis of autosomal dominant Robinow syndrome due to novel DVL1 variant. Prenatal diagnosis 44 (9) (2024)
Carly M Smith, Kristi Guinon, Suha Bachir, Christina G Tise
Fetal phenotype and diagnosis of autosomal dominant Robinow syndrome due to novel DVL1 variant. Prenatal diagnosis (2024)
Courtney P Verscaj, Carly M Smith, Margaret Homeyer, Dena R Matalon
Raine syndrome: Prenatally identified severe craniofacial phenotype with multisuture synostosis and brain abnormalities associated with variants in FAM20C. Prenatal diagnosis (2024)
Courtney P Verscaj, Carly M Smith, Margaret Homeyer, Dena R Matalon
Raine syndrome: Prenatally identified severe craniofacial phenotype with multisuture synostosis and brain abnormalities associated with variants in FAM20C. Prenatal diagnosis 44 (3) (2024)
Carly M Smith, Kristi Guinon, Suha Bachir, Christina G Tise
Fetal phenotype and diagnosis of autosomal dominant Robinow syndrome due to novel DVL1 variant. Prenatal diagnosis 44 (9) (2024)