Ana Beleza Meireles

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Novel truncating mutations in CTNND1 cause a dominant craniofacial and cardiac syndrome
Alharatani, R., Ververi, A., Beleza-Meireles, A., Ji, W., Mis, E., Patterson, Q. T., Griffin, J. N., Bhujel, N., Chang, C. A., Dixit, A., Konstantino, M., Healy, C., Hannan, S., Neo, N., Cash, A., Li, D., Bhoj, E., Zackai, E. H., Cleaver, R. & Baralle, D. & 10 others, McEntagart, M., Newbury-Ecob, R., Scott, R., Hurst, J. A., Au, P. Y. B., Hosey, M. T., Khokha, M., Marciano, D. K., Lakhani, S. A. & Liu, K. J., 21 Jul 2020, In: Human Molecular Genetics. 29, 11, p. 1900-1921 22 p.
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Ana Beleza Meireles

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Novel truncating mutations in CTNND1 cause a dominant craniofacial and cardiac syndrome