Variants in PHF8 cause a spectrum of X-linked neurodevelopmental disorders and facial dysmorphology

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Detalles Bibliográficos
Autores principales: Sobering, Andrew K., Bryant, Laura M., Li, Dong, McGaughran, Julie, Maystadt, Isabelle, Moortgat, Stephanie, Graham, John M., van Haeringen, Arie, Ruivenkamp, Claudia, Cuperus, Roos, Vogt, Julie, Morton, Jenny, Brasch-Andersen, Charlotte, Steenhof, Maria, Hansen, Lars Kjærsgaard, Adler, Élodie, Lyonnet, Stanislas, Pingault, Veronique, Sandrine, Marlin, Ziegler, Alban, Donald, Tyhiesia, Nelson, Beverly, Holt, Brandon, Petryna, Oleksandra, Firth, Helen, McWalter, Kirsty, Zyskind, Jacob, Telegrafi, Aida, Juusola, Jane, Person, Richard, Bamshad, Michael J., Earl, Dawn, Chun-Hui Tsai, Anne, Yearwood, Katherine R., Marco, Elysa, Nowak, Catherine, Douglas, Jessica, Hakonarson, Hakon, Bhoj, Elizabeth J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Correction
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9792386/
https://www.ncbi.nlm.nih.gov/pubmed/36583168
http://dx.doi.org/10.1016/j.xhgg.2022.100168

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9792386/
https://www.ncbi.nlm.nih.gov/pubmed/36583168
http://dx.doi.org/10.1016/j.xhgg.2022.100168

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