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A Comprehensive Review of Pediatric Tumors and Associated Cancer Predisposition Syndromes.

artículo científico publicado en 2017

Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine

artículo científico publicado en 2016

Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine

article

Diagnostic Yield of Clinical Tumor and Germline Whole-Exome Sequencing for Children With Solid Tumors

artículo científico publicado en 2016

Genomic Sequencing Results Disclosure in Diverse and Medically Underserved Populations: Themes, Challenges, and Strategies from the CSER Consortium

artículo científico publicado en 2021

Germline POLE mutation in a child with hypermutated medulloblastoma and features of constitutional mismatch repair deficiency

scientific article published on 23 October 2019

Haploinsufficiency of STK11 and neighboring genes cause a contiguous gene syndrome including Peutz–Jeghers phenotype ⬇️

artículo científico publicado el 14 de septiembre de 2012

Obtaining informed consent for clinical tumor and germline exome sequencing of newly diagnosed childhood cancer patients

artículo científico publicado en 2014

Pediatric Cancer Genetics Research and an Evolving Preventive Ethics Approach for Return of Results after Death of the Subject

artículo científico publicado en 2015

Phenotypic differences in Juvenile Polyposis Syndrome with or without a disease-causing SMAD4/BMPR1A variant

artículo científico publicado en 2020

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