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Carolyn R Serbinski

7PUBLICATIONS
7CO-AUTHORS
MultimorbidityNeurology and neuromuscular diseasesDevelopmental genetics (incl. sex determination)NeurogeneticsMedical devices
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Publications (7)

Sort by Publication Date:
|Nov 11, 2025
Syndrome of the Month: An Update on Smith-Kingsmore Syndrome: Characterization of Developmental Milestones and a Review of the Literature.

Carolyn R Raski, Carlos E Prada

|Aug 29, 2025
Sacroiliac Joint Involvement: An Underreported Complication of NF1.

Jenny P Garzon, Eva Dombi, Jonathan Samet

|Sep 11, 2024
Further Delineation of the Proximal 16p11.2 Microdeletion Syndrome: Novel Findings Among 22 New Individuals.

Anne M McRae, Jaime Duncan, Andy Drackley

|Jul 18, 2024
Expanding the phenotype of neurofibromatosis type 1 microdeletion syndrome.

Jenny P Garzon, Andrea Patete, Lindsey Aschbacher-Smith

|May 18, 2024
Dandy-Walker malformation in an individual with ABL1 variant.

Jenny P Garzon, Andrea C Pardo, Carolyn R Raski

|May 09, 2024
Aminotransferase trends in propionic acidemia.

Maria P Silva, Carolyn R Raski, Joel Charrow

Pageof 2

Frequent Collaborators

3 joint publications

Carlos E Prada

3 joint publications

Jenny P Garzon

2 joint publications

Maria P Silva

2 joint publications

Andy Drackley

1 joint publications

Anne M McRae

1 joint publications

Alexander Ing

1 joint publications

K Nicole Weaver

Frequent Collaborators

3 joint publications

Carlos E Prada

3 joint publications

Jenny P Garzon

2 joint publications

Maria P Silva

2 joint publications

Andy Drackley

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