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| Next generation sequencing and array-based comparative genomic hybridization for molecular diagnosis of pediatric endocrine disorders | |
| Maki Fukami, Mami Miyado | |
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Ann Pediatr Endocrinol Metab. 2017;22(2):90-94. Published online June 28, 2017 DOI: https://doi.org/10.6065/apem.2017.22.2.90 |
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Next generation sequencing and array-based comparative genomic hybridization for molecular diagnosis of pediatric endocrine disorders Annals of Pediatric Endocrinology & Metabolism. 2017;22(2):90  The Next Generation Sequencing Based Molecular Diagnosis of Visual Diseases Next Generation Sequencing Based Clinical Molecular Diagnosis of Human Genetic Disorders. 2017;51-69 Next-Generation Sequencing Based Clinical Molecular Diagnosis of Primary Immunodeficiency Diseases Next Generation Sequencing Based Clinical Molecular Diagnosis of Human Genetic Disorders. 2017;89-112 Family-Based Next-Generation Sequencing Analysis Next Generation Sequencing Based Clinical Molecular Diagnosis of Human Genetic Disorders. 2017;321-338 Overview of the Clinical Utility of Next Generation Sequencing in Molecular Diagnoses of Human Genetic Disorders Next Generation Sequencing Based Clinical Molecular Diagnosis of Human Genetic Disorders. 2017;1-11 Validation of Next-Generation Sequencing and Array Comparative Genomic Hybridization for Diagnosis and Screening of Reciprocal and Robertsonian Translocations in Human Blastocysts . 2020; Next-Generation Sequencing for the Diagnosis of Monogenic Disorders of Insulin Secretion Next Generation Sequencing Based Clinical Molecular Diagnosis of Human Genetic Disorders. 2017;201-242 Next Generation Sequencing (NGS) Based Panel Analysis of Metabolic Pathways Next Generation Sequencing Based Clinical Molecular Diagnosis of Human Genetic Disorders. 2017;23-49 Next-Generation Sequencing Based Testing for Disorders of the Skeleton Next Generation Sequencing Based Clinical Molecular Diagnosis of Human Genetic Disorders. 2017;113-121 Next Generation of Carrier Screening Next Generation Sequencing Based Clinical Molecular Diagnosis of Human Genetic Disorders. 2017;339-354 |
