Linked-read genome sequencing identifies biallelic pathogenic variants in DONSON as a novel cause of Meier-Gorlin syndrome

出版年份 2019 全文链接

标题

Linked-read genome sequencing identifies biallelic pathogenic variants in DONSON as a novel cause of Meier-Gorlin syndrome

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关键词

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出版物

JOURNAL OF MEDICAL GENETICS

Volume -, Issue -, Pages jmedgenet-2019-106396

出版商

BMJ

发表日期

2019-11-30

DOI

10.1136/jmedgenet-2019-106396

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