De novo and biallelic DEAF1 variants cause a phenotypic spectrum.
Document Type
Journal Article
Publication Date
3-29-2019
Journal
Genetics in medicine : official journal of the American College of Medical Genetics
DOI
10.1038/s41436-019-0473-6
APA Citation
Nabais Sá, M., Jensik, P., McGee, S., Parker, M., Lahiri, N., McNeil, E., Kroes, H., Hagerman, R., Harrison, R., Montgomery, T., Splitt, M., Palmer, E., Sachdev, R., Mefford, H., Scott, A., Martinez-Agosto, J., Lorenz, R., Orenstein, N., Berg, J., Amiel, J., Heron, D., Keren, B., Cobben, J., Menke, L., Marco, E., Graham, J., Pierson, T., Karimiani, E., Maroofian, R., Manzini, M., Cauley, E., Colombo, R., Odent, S., Dubourg, C., Phornphutkul, C., de Brouwer, A., de Vries, B., & Vulto-vanSilfhout, A. (2019). De novo and biallelic DEAF1 variants cause a phenotypic spectrum.. Genetics in medicine : official journal of the American College of Medical Genetics, (). http://dx.doi.org/10.1038/s41436-019-0473-6
Peer Reviewed
1
Comments
Epub ahead of print