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新搜索筛选: 出版者 Wiley ✖ 删除限定条件出版者: Wiley

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<span itemprop="name">Whole exome sequencing and co-expression analysis identify an SCN1A variant that modifies pathogenicity in a family with genetic epilepsy and febrile seizures plus </span>

<span itemprop="name">Loeys-Dietz syndrome caused by 1q41 deletion including TGFβ2 is associated with a neurodevelopmental phenotype</span>

<span itemprop="name">Gigantic genomes of salamanders indicate body temperature, not genome size, is the driver of global methylation and 5-methylcytosine deamination in vertebrates</span>

Whole exome sequencing and co-expression analysis identify an SCN1A variant that modifies pathogenicity in a family with genetic epilepsy and febrile seizures plus

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Loeys-Dietz syndrome caused by 1q41 deletion including TGFβ2 is associated with a neurodevelopmental phenotype

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Gigantic genomes of salamanders indicate body temperature, not genome size, is the driver of global methylation and 5-methylcytosine deamination in vertebrates

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Work3

Article3

Steding, Catherine1
Adams, A. N.1
Afawi, Z.1
Cumbay, Medhane1
Cummins, T.1
更多创造者s »

1q41 deletion1
SCN1A-related epilepsy1
CpG dinucleotides1
Loeys-Dietz syndrome1
TGFB21
更多关键词s »

English3

Wiley[删除]3
International League Against Epilepsy1
Society for the Study of Evolution1

Current results range from 2022 to 2022

Date Created range begin Date Created range end

Faculty Publications and Research - MUCOM2
Department of Biology1

Marian University3