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Novel mutation in ENG gene causing Hereditary Hemorrhagic Telangiectasia in a Peruvian family
(Sociedade Brasileira de Genética, 2020)
Acceso abierto
Hereditary Hemorrhagic Telangiectasia (HHT) is a rare disorder of vascular development. Common manifestations include epistaxis, telangiectasias and arteriovenous malformations (AVMs) in multiple organs. Most patients have ...
A paleogenomic reconstruction of the deep population history of the andes
(Elsevier, 2020-05-06)
Acceso abierto
There are many unanswered questions about the population history of the Central and South Central Andes, particularly regarding the impact of large-scale societies, such as the Moche, Wari, Tiwanaku, and Inca. We assembled ...
Precision medicine for locally advanced breast cancer: frontiers and challenges in Latin America
(ECancer Medical Science, 2019-01-22)
Acceso abierto
Advances in high-throughput technologies and their involvement in the ‘omics’ of cancer have made possible the identification of hundreds of biomarkers and the development of predictive and prognostic platforms that model ...