Matteson, Paul

Center for Advanced Biotechnology and Medicine Piscataway New Jersey USA

1 paper on CoChat

Most cited papers

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Biallelic hypomorphic variants in ALDH1A2 cause a novel lethal human multiple congenital anomaly syndrome encompassing diaphragmatic, pulmonary, and cardiovascular defects
Beecroft, S. J., Ayala, M., McGillivray, G., Nanda, V., Agolini, E., Novelli, A., Digilio, M. C., Dotta, A., Carrozzo, R., Clayton, J., et al. (2021) · Human Mutation
Genomics and Rare DiseasesCongenital heart defects research
Cited by 25

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