Gaffney, Lydia

Royal Women's Hospital · Victorian Clinical Genetics Services · Murdoch Children's Research Institute

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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