使用本網站需要啟用 JavaScript, 請啟用后刷新頁面獲得更好的體驗
亚洲精品午夜精品,日本二手网站,国产AⅤ爽AV久久久久成人社区,日本一二三区不收费av
<ul id="jms49"></ul>
登錄
注冊
首頁
個人居家檢測
臨床應用研究
科研合作項目
合作與服務
社區
純合片段分析
姓氏祖源
祖源平均臉
基因關系
基因保險助手
原始數據
使用 WeGene 需要啟用 Cookies, 請啟用后刷新頁面獲得更好的體驗
社區首頁
小組
近視
近視
發起討論
近視
1 個討論
只看精華帖
按熱門排序
按最新排序
暫時沒有精華內容
發起討論
近視
1 個討論
相關基因
TYR
位點：RS1042602
ARMS2
位點：RS10490924
RBFOX1
位點：RS10500355
TJP2
位點：RS11145465
LAMA2
位點：RS12193446
C14orf39
位點：RS1254319
SIX6
位點：RS146737847
位點：RS33912345
BMP4
位點：RS17563
位點：RS2855530
GSDMA
位點：RS3894194
位點：RS7212938
GNB3
位點：RS5442
MIR6130
位點：RS7042950
FLT1
位點：RS7337610
KCNQ5
位點：RS7744813
PDE11A
位點：RS17400325
位點：RS2573081
PTPN5
位點：RS1550870
HIVEP3
位點：RS11210537
KIRREL
位點：RS11802995
PRSS56
位點：RS1550094
ZBTB38
位點：RS7624084
COL10A1
位點：RS1064583
CASC15
位點：RS1207782
VIPR2
位點：RS17837871
BICC1
位點：RS1649068
DLG2
位點：RS2155413
GRIN2B
位點：RS4764038
CPSF2
位點：RS56014528
RASGRF1
位點：RS6495367
SHISA6
位點：RS2908972
MYO5B
位點：RS12965607
BMP3
位點：RS74764079
KAZALD1
位點：RS807037
COL4A4
位點：RS2229814
SNTB1
位點：RS7839488
Insights into the genetic basis of retinal detachment
Whole exome sequence analysis in 51624 participants identifies novel genes and variants associated with refractive error and myopia
Meta-analysis of genome-wide association studies in five cohorts reveals common variants in RBFOX1, a regulator of tissue-specific splicing, associated with refractive error
Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error
Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error
Whole exome sequence analysis in 51624 participants identifies novel genes and variants associated with refractive error and myopia
Whole exome sequence analysis in 51624 participants identifies novel genes and variants associated with refractive error and myopia
Whole exome sequence analysis in 51624 participants identifies novel genes and variants associated with refractive error and myopia
Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error
Whole exome sequence analysis in 51624 participants identifies novel genes and variants associated with refractive error and myopia
Whole exome sequence analysis in 51624 participants identifies novel genes and variants associated with refractive error and myopia
Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error
Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error
Whole exome sequence analysis in 51624 participants identifies novel genes and variants associated with refractive error and myopia
Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error
Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error
Detection and interpretation of shared genetic influences on 42 human traits
Detection and interpretation of shared genetic influences on 42 human traits
Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error
Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error
Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error
Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error
Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error
Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error
Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error
Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error
Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error
Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error
Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error
Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error
Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error
Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error
Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error
Insights into the genetic basis of retinal detachment
Whole exome sequence analysis in 51624 participants identifies novel genes and variants associated with refractive error and myopia
Whole exome sequence analysis in 51624 participants identifies novel genes and variants associated with refractive error and myopia
Association of the ZC3H11B, ZFHX1B and SNTB1 genes with myopia of different severities
查看參考文獻
首頁
個人基因檢測
臨床應用研究
科研合作項目
合作與服務
示例報告
下載 APP
社區
關于 WeGene
關于我們
媒體新聞
倫理委員會
隱私協議
加入我們
服務協議
價格保護
幫助中心
關于基因檢測
賬戶購買
樣本寄送
報告解讀
隱私安全
關于第三方數據
社區分享
開放平臺
申請成為開發者
開發文檔
客服微信公眾號
聯系我們
客服郵箱：
service@wegene.com
合作咨詢：
partner@wegene.com
© 2025 WeGene. All Rights Reserved
深圳市市場監督管理局企業主體身份公示
|
粵ICP備15012185號
| 互聯網藥品信息服務資格證書:（粵）-非經營性-2023-0379
中文
English
<track id="ffr4e"></track>
<dfn id="ffr4e"></dfn>
主站蜘蛛池模板：
东丽区
|
康乐县
|
新泰市
|
顺义区
|
镶黄旗
|
鹤壁市
|
徐闻县
|
句容市
|
旅游
|
仁化县
|
阜宁县
|
乌什县
|
炉霍县
|
乐昌市
|
鲁甸县
|
岢岚县
|
汉源县
|
崇文区
|
龙泉市
|
临清市
|
女性
|
保康县
|
古丈县
|
上高县
|
宣化县
|
玉溪市
|
肥城市
|
扬中市
|
兖州市
|
鹤峰县
|
海城市
|
洮南市
|
合江县
|
宜黄县
|
龙山县
|
临桂县
|
宽城
|
天峻县
|
余干县
|
南通市
|
寿宁县
|
<menu id="ozewr"></menu>
<menu id="ozewr"></menu>
<menu id="ozewr"><span id="ozewr"></span></menu>
純合片段分析
姓氏祖源
祖源平均臉
基因關系
基因保險助手
原始數據
深圳市市場監督管理局企業主體身份公示
中文
English