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sisea
Lv7
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3915 积分
2021-08-02 加入
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Genetic variant interpretation for the neurologist - A pragmatic approach in the next-generation sequencing era in childhood epilepsy
2天前
已完结
Genetic testing for unexplained epilepsy: A review of diagnostic approach, benefits, and referral algorithm
2天前
已完结
Genomic testing and molecular diagnosis among infants with congenital heart disease in the neonatal intensive care unit
8天前
已完结
Fifteen-minute consultation: The efficient investigation of infantile and childhood epileptic encephalopathies in the era of modern genomics
9天前
已完结
Diagnostic Yield of Whole Genome Sequencing After Nondiagnostic Exome Sequencing or Gene Panel in Developmental and Epileptic Encephalopathies
10天前
已完结
Clinical Application of Targeted Next-Generation Sequencing Panels and Whole Exome Sequencing in Childhood Epilepsy
13天前
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Optical genome mapping for prenatal diagnosis: A prospective study
17天前
已完结
Comparison of different methods of screening for preterm pre-eclampsia: cohort study
23天前
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Using implementation science to evaluate a population-wide genomic screening program: Findings from the first 20,000 In Our DNA SC participants
1个月前
已完结
Newborn screening for primary carnitine deficiency using a second-tier genetic test
1个月前
已完结
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