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Publications by Yanting Xu
The Genomic Mutation Spectrums of Breast Fibroadenomas in Chinese Population by Whole Exome Sequencing Analysis
Cancer Medicine
Cancer Research
Nuclear Medicine
Radiology
Imaging
Oncology
Related publications
Whole-Exome Sequencing Analysis of Waardenburg Syndrome in a Chinese Family
Human Genome Variation
Biochemistry
Genetics
Molecular Biology
Clinical Cancer Genomic Profiling by Three-Platform Sequencing of Whole Genome, Whole Exome and Transcriptome
Nature Communications
Astronomy
Genetics
Molecular Biology
Biochemistry
Chemistry
Physics
Whole Exome Sequencing in Monogenic Dyslipidemias
Journal of Atherosclerosis and Thrombosis
Biochemistry
Internal Medicine
Cardiovascular Medicine
Cardiology
Whole-Genome Sequencing Is More Powerful Than Whole-Exome Sequencing for Detecting Exome Variants
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
A De Novo Heterozygous Frameshift Mutation Identified in BCL11B Causes Neurodevelopmental Disorder by Whole Exome Sequencing
Molecular genetics & genomic medicine
Genetics
Molecular Biology
Revealing Genomic Profile That Underlies Tropism of Myeloma Cells Using Whole Exome Sequencing
Clinical Lymphoma, Myeloma and Leukemia
Cancer Research
Oncology
Hematology
Clinical Application of Whole-Exome Sequencing
JAMA Neurology
Neurology
Diagnosis by Sequencing: Correction of Misdiagnosis From FSHD2 to LGMD2A by Whole-Exome Analysis
European Journal of Human Genetics
Genetics
Whole-Exome Sequencing in the Investigation of Retinal Dystrophy
The Lancet
Medicine