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[PDF][PDF] Burden testing of rare variants identified through exome sequencing via publicly available control data

MH Guo, L Plummer, YM Chan, JN Hirschhorn… - The American Journal of …, 2018 - cell.com

The genetic causes of many Mendelian disorders remain undefined. Factors such as lack of
large multiplex families, locus heterogeneity, and incomplete penetrance hamper these …

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[HTML][HTML] Burden Testing of Rare Variants Identified through Exome Sequencing via Publicly Available Control Data

MH Guo, L Plummer, YM Chan, JN Hirschhorn… - The American Journal of …, 2018 - Elsevier

The genetic causes of many Mendelian disorders remain undefined. Factors such as lack of
large multiplex families, locus heterogeneity, and incomplete penetrance hamper these …

[引用][C] Burden Testing of Rare Variants Identified through Exome Sequencing via Publicly Available Control Data

MH Guo, L Plummer, YM Chan, JN Hirschhorn… - The American Journal …, 2018 - cir.nii.ac.jp

Burden Testing of Rare Variants Identified through Exome Sequencing via Publicly Available
Control Data | CiNii Research CiNii 国立情報学研究所学術情報ナビゲータ[サイニィ] 詳細へ移動 …

Burden Testing of Rare Variants Identified through Exome Sequencing via Publicly Available Control Data

MH Guo, L Plummer, YM Chan… - … journal of human …, 2018 - pubmed.ncbi.nlm.nih.gov

The genetic causes of many Mendelian disorders remain undefined. Factors such as lack of
large multiplex families, locus heterogeneity, and incomplete penetrance hamper these …

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[PDF][PDF] Burden testing of rare variants identified through exome sequencing via publicly available control data

[HTML][HTML] Burden Testing of Rare Variants Identified through Exome Sequencing via Publicly Available Control Data

[引用][C] Burden Testing of Rare Variants Identified through Exome Sequencing via Publicly Available Control Data

Burden Testing of Rare Variants Identified through Exome Sequencing via Publicly Available Control Data

[HTML][HTML] Burden Testing of Rare Variants Identified through Exome Sequencing via Publicly Available Control Data

Burden Testing of Rare Variants Identified through Exome Sequencing via Publicly Available Control Data.

Burden Testing of Rare Variants Identified through Exome Sequencing via Publicly Available Control Data.

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