about
Challenges of deciphering gastric cancer heterogeneityClinical application of next-generation sequencing for Mendelian diseasesThe Human Genome Project, and recent advances in personalized genomicsGenetic epidemiology and nonsyndromic structural birth defects: from candidate genes to epigeneticsGenomics, personalized medicine, and pediatricsTumor heterogeneity and resistance to EGFR-targeted therapy in advanced nonsmall cell lung cancer: challenges and perspectivesDeveloping context-specific next-generation sequencing policyClinical interpretation of CNVs with cross-species phenotype dataBioethical issues of preventing hereditary diseases with late onset in the Sakha Republic (Yakutia)HIV, Aging, and Viral Coinfections: Taking the Long View.Solute Carrier Family 26 Member a2 (slc26a2) Regulates Otic Development and Hair Cell Survival in Zebrafish.Design and implementation of a randomized controlled trial of genomic counseling for patients with chronic disease.Integrated RNA and DNA sequencing improves mutation detection in low purity tumors.Translating personalized medicine using new genetic technologies in clinical practice: the ethical issuesBiomarker testing for breast, lung, and gastroesophageal cancers at NCI designated cancer centers.Introducing a New Competency Into Nursing PracticeManaging large-scale genomic datasets and translation into clinical practice.Medical care costs incurred by patients with smoking-related non-small cell lung cancer treated at the National Cancer Institute of Mexico.Challenges of coverage policy development for next-generation tumor sequencing panels: experts and payers weigh in.Reporting Incidental Findings in Genomic Scale Clinical Sequencing-A Clinical Laboratory Perspective: A Report of the Association for Molecular Pathology.Precision Medicine for Continuing Phenotype Expansion of Human Genetic Diseases.Use of Targeted Exome Sequencing for Molecular Diagnosis of Skeletal DisordersPhenotype-driven gene target definition in clinical genome-wide sequencing data interpretation.Genetic testing and genomic analysis: a debate on ethical, social and legal issues in the Arab world with a focus on QatarDiagnosis of D-Bifunctional Protein Deficiency through Whole-Genome Sequencing: Implications for Cost-Effective Care.Association of Arrhythmia-Related Genetic Variants With Phenotypes Documented in Electronic Medical Records.Whole-genome association analysis of treatment response in obsessive-compulsive disorder.National Institutes of Health Center for Regenerative Medicine: putting science into practice.Factors and processes modulating phenotypes in neuronopathic lysosomal storage diseases.Development and validation of risk models and molecular diagnostics to permit personalized management of cancer.Application of capillary electrophoresis for the early diagnosis of cancer.Considerations for rare variants in drug metabolism genes and the clinical implications.Whole exome or genome sequencing: nurses need to prepare families for the possibilities.Genomic sciences for developmentalists: a merge of science and practice.Building the foundation for genomics in precision medicine.Genetics and the placebo effect: the placebome.Genome-Wide Sequencing for Prenatal Detection of Fetal Single-Gene Disorders.Animal medical genetics: a perspective on the epidemiology and control of inherited disorders.Tissue Engineering Strategies as Tools for Personalized Meningioma Treatment.Identification of false-negative mutations missed by next-generation sequencing in retinitis pigmentosa patients: a complementary approach to clinical genetic diagnostic testing.
P2860
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P2860
description
2013 nî lūn-bûn
@nan
2013 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2013 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
name
New approaches to molecular diagnosis.
@ast
New approaches to molecular diagnosis.
@en
New approaches to molecular diagnosis.
@nl
type
label
New approaches to molecular diagnosis.
@ast
New approaches to molecular diagnosis.
@en
New approaches to molecular diagnosis.
@nl
prefLabel
New approaches to molecular diagnosis.
@ast
New approaches to molecular diagnosis.
@en
New approaches to molecular diagnosis.
@nl
P356
P1476
New approaches to molecular diagnosis.
@en
P2093
Bruce R Korf
P304
P356
10.1001/JAMA.2013.3239
P407
P577
2013-04-01T00:00:00Z