Human disease genes website series: An international, open and dynamic library for up‐to‐date clinical information

Since the introduction of next‐generation sequencing, an increasing number of disorders have been discovered to have genetic etiology. To address diverse clinical questions and coordinate research activities that arise with the identification of these rare disorders, we developed the Human Disease G...

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Detalles Bibliográficos
Autores principales: Dingemans, Alexander J. M., Stremmelaar, Diante E., Vissers, Lisenka E. L. M., Jansen, Sandra, Nabais Sá, Maria J., van Remortele, Angela, Jonis, Noraly, Truijen, Kim, van de Ven, Sam, Ewals, Jeroen, Verbruggen, Michel, Koolen, David A., Brunner, Han G., Eichler, Evan E., Gecz, Jozef, de Vries, Bert B. A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2021
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7986414/
https://www.ncbi.nlm.nih.gov/pubmed/33439542
http://dx.doi.org/10.1002/ajmg.a.62057

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7986414/
https://www.ncbi.nlm.nih.gov/pubmed/33439542
http://dx.doi.org/10.1002/ajmg.a.62057

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