Rogers, Carolyn

Hunter Genetics

1 paper on CoChatORCID 0000-0001-8906-8420

Most cited papers

Verified
CCDC22 mutations that impair COMMD binding cause attenuated 3C/Ritscher-Schinzel syndrome
Singla, A., Rogers, C., Touma, M.-J., El-Najjar, Y., Colley, A., Boesch, D. J., Billadeau, D. D., Gecz, J., Chen, B., & Burstein, E. (2025) · BMC Medical Genomics
Cellular transport and secretionGenomics and Rare Diseases
Cited by 1

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