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杜氏肌營養(yǎng)不良癥
杜氏肌營養(yǎng)不良癥
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杜氏肌營養(yǎng)不良癥
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作為攜帶多個突變的男性，是不是墳頭草應該已經(jīng)好幾米了。。。
nagakaze
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moonxoyo
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2020-06-28 18:44
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杜氏肌營養(yǎng)不良癥
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相關(guān)基因
DMD
位點：RS104894787
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DMD, DMD
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ClinVar: public archive of interpretations of clinically relevant variants.
ClinVar: public archive of interpretations of clinically relevant variants.
ClinVar: public archive of interpretations of clinically relevant variants.
ClinVar: public archive of interpretations of clinically relevant variants.
ClinVar: public archive of interpretations of clinically relevant variants.
ClinVar: public archive of interpretations of clinically relevant variants.
ClinVar: public archive of interpretations of clinically relevant variants.
ClinVar: public archive of interpretations of clinically relevant variants.
ClinVar: public archive of interpretations of clinically relevant variants.
ClinVar: public archive of interpretations of clinically relevant variants.
ClinVar: public archive of interpretations of clinically relevant variants.
ClinVar: public archive of interpretations of clinically relevant variants.
ClinVar: public archive of interpretations of clinically relevant variants.
ClinVar: public archive of interpretations of clinically relevant variants.
ClinVar: public archive of interpretations of clinically relevant variants.
ClinVar: public archive of interpretations of clinically relevant variants.
ClinVar: public archive of interpretations of clinically relevant variants.
ClinVar: public archive of interpretations of clinically relevant variants.
ClinVar: public archive of interpretations of clinically relevant variants.
ClinVar: public archive of interpretations of clinically relevant variants.
ClinVar: public archive of interpretations of clinically relevant variants.
ClinVar: public archive of interpretations of clinically relevant variants.
ClinVar: public archive of interpretations of clinically relevant variants.
ClinVar: public archive of interpretations of clinically relevant variants.
ClinVar: public archive of interpretations of clinically relevant variants.
ClinVar: public archive of interpretations of clinically relevant variants.
ClinVar: public archive of interpretations of clinically relevant variants.
ClinVar: public archive of interpretations of clinically relevant variants.
ClinVar: public archive of interpretations of clinically relevant variants.
ClinVar: public archive of interpretations of clinically relevant variants.
ClinVar: public archive of interpretations of clinically relevant variants.
ClinVar: public archive of interpretations of clinically relevant variants.
ClinVar: public archive of interpretations of clinically relevant variants.
ClinVar: public archive of interpretations of clinically relevant variants.
ClinVar: public archive of interpretations of clinically relevant variants.
ClinVar: public archive of interpretations of clinically relevant variants.
ClinVar: public archive of interpretations of clinically relevant variants.
ClinVar: public archive of interpretations of clinically relevant variants.
ClinVar: public archive of interpretations of clinically relevant variants.
ClinVar: public archive of interpretations of clinically relevant variants.
ClinVar: public archive of interpretations of clinically relevant variants.
ClinVar: public archive of interpretations of clinically relevant variants.
ClinVar: public archive of interpretations of clinically relevant variants.
ClinVar: public archive of interpretations of clinically relevant variants.
ClinVar: public archive of interpretations of clinically relevant variants.
ClinVar: public archive of interpretations of clinically relevant variants.
ClinVar: public archive of interpretations of clinically relevant variants.
ClinVar: public archive of interpretations of clinically relevant variants.
ClinVar: public archive of interpretations of clinically relevant variants.
ClinVar: public archive of interpretations of clinically relevant variants.
ClinVar: public archive of interpretations of clinically relevant variants.
ClinVar: public archive of interpretations of clinically relevant variants.
ClinVar: public archive of interpretations of clinically relevant variants.
ClinVar: public archive of interpretations of clinically relevant variants.
ClinVar: public archive of interpretations of clinically relevant variants.
ClinVar: public archive of interpretations of clinically relevant variants.
ClinVar: public archive of interpretations of clinically relevant variants.
ClinVar: public archive of interpretations of clinically relevant variants.
ClinVar: public archive of interpretations of clinically relevant variants.
ClinVar: public archive of interpretations of clinically relevant variants.
ClinVar: public archive of interpretations of clinically relevant variants.
ClinVar: public archive of interpretations of clinically relevant variants.
ClinVar: public archive of interpretations of clinically relevant variants.
ClinVar: public archive of interpretations of clinically relevant variants.
ClinVar: public archive of interpretations of clinically relevant variants.
ClinVar: public archive of interpretations of clinically relevant variants.
ClinVar: public archive of interpretations of clinically relevant variants.
ClinVar: public archive of interpretations of clinically relevant variants.
ClinVar: public archive of interpretations of clinically relevant variants.
ClinVar: public archive of interpretations of clinically relevant variants.
ClinVar: public archive of interpretations of clinically relevant variants.
ClinVar: public archive of interpretations of clinically relevant variants.
ClinVar: public archive of interpretations of clinically relevant variants.
ClinVar: public archive of interpretations of clinically relevant variants.
ClinVar: public archive of interpretations of clinically relevant variants.
ClinVar: public archive of interpretations of clinically relevant variants.
ClinVar: public archive of interpretations of clinically relevant variants.
ClinVar: public archive of interpretations of clinically relevant variants.
ClinVar: public archive of interpretations of clinically relevant variants.
ClinVar: public archive of interpretations of clinically relevant variants.
ClinVar: public archive of interpretations of clinically relevant variants.
ClinVar: public archive of interpretations of clinically relevant variants.
ClinVar: public archive of interpretations of clinically relevant variants.
ClinVar: public archive of interpretations of clinically relevant variants.
ClinVar: public archive of interpretations of clinically relevant variants.
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純合片段分析
姓氏祖源
祖源平均臉
基因關(guān)系
基因保險助手
原始數(shù)據(jù)
深圳市市場監(jiān)督管理局企業(yè)主體身份公示
中文
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