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Genetic Variants for Long QT Syndrome among Infants and Children from a Statewide Newborn Hearing Screening Program Cohort
by
Chang, Ruey-Kang R., MD, MPH
,
Lan, Yueh-Tze, MD
,
Silka, Michael J., MD
,
Morrow, Hallie, MD
,
Kwong, Alan, MS
,
Smith-Lang, Janna, PhD
,
Wallerstein, Robert, MD
,
Lin, Henry J., MD
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The Journal of pediatrics
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The Journal Of Pediatrics
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The Journal Of Pediatrics/The Journal Of Pediatrics
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Alternative Splicing
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Child, Preschool
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Electrocardiography
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Genetic Testing
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Hearing Loss - Diagnosis
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Hearing Loss - Genetics
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Heterozygote
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Humans
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Infant
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Infant, Newborn
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Jervell-Lange Nielsen Syndrome - Genetics
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Kcnq1 Potassium Channel - Genetics
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Life Sciences & Biomedicine
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Long Qt Syndrome - Genetics
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Mutation
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Nav1.5 Voltage-Gated Sodium Channel - Genetics
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Neonatal Screening
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Pediatrics
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Polymorphism, Genetic
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Prospective Studies
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