Megan Samuels
2PUBLICATIONS
1CO-AUTHORS

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Publications (2)
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|Feb 05, 2025
Rapid Whole Genome Sequencing Uncovers a Triple Diagnosis: X-Linked Chondrodysplasia Punctata, MECP2-Related Disorder, and Mosaic Jacobs Syndrome.Megan Samuels, Kathleen Shields, Paul Hillman
|Jun 07, 2024
Noonan syndrome and type 1 Chiari malformation: Possible association.Megan Samuels, Hope Northrup
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