Implementation of massive sequencing in the genetic diagnosis of hereditary cancer syndromes: diagnostic performance in the Hereditary Cancer Programme of the Valencia Community (FamCan-NGS). Ramírez-Calvo, M., García-Casado, Z., Fernández-Serra, A., de Juan, I., Palanca, S., Oltra, S., Soto, J. L., Castillejo, A., Barbera, V. M., & Juan-Fita, M. J. Hereditary cancer in clinical practice, 17(1):3, January, 2019.
Implementation of massive sequencing in the genetic diagnosis of hereditary cancer syndromes: diagnostic performance in the Hereditary Cancer Programme of the Valencia Community (FamCan-NGS) [link]Paper  bibtex   
@article{ramirez-calvo_implementation_2019,
	title = {Implementation of massive sequencing in the genetic diagnosis of hereditary cancer syndromes: diagnostic performance in the {Hereditary} {Cancer} {Programme} of the {Valencia} {Community} ({FamCan}-{NGS})},
	volume = {17},
	shorttitle = {Implementation of massive sequencing in the genetic diagnosis of hereditary cancer syndromes},
	url = {https://link.springer.com/article/10.1186/s13053-019-0104-x},
	number = {1},
	journal = {Hereditary cancer in clinical practice},
	author = {Ramírez-Calvo, Marta and García-Casado, Zaida and Fernández-Serra, Antonio and de Juan, Inmaculada and Palanca, Sarai and Oltra, Silvestre and Soto, José Luis and Castillejo, Adela and Barbera, Víctor M. and Juan-Fita, Ma José},
	month = jan,
	year = {2019},
	keywords = {Genomics, HCS, Hereditary Disorders, SNV, SOPHiA DDM, Targeted},
	pages = {3},
}

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