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Chinese Gene Variation Database

The Chinese Gene Variation Database (CGVdb) is established to collect genetic mutations and other variations information in the Chinese population for clinical application and medical genetic research. Contents and structure of this ethnic mutation database follow the guidelines. Recommended by HUGO Human Genome Variation Society (HGVS). A natural language processing program for annotating the discussed human genes in biomedical texts. CGVdb 1997 - 1998 data now online (Demonstrate Only).

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Chinese Gene Variation Database | cgvdb.tw Reviews
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The Chinese Gene Variation Database (CGVdb) is established to collect genetic mutations and other variations information in the Chinese population for clinical application and medical genetic research. Contents and structure of this ethnic mutation database follow the guidelines. Recommended by HUGO Human Genome Variation Society (HGVS). A natural language processing program for annotating the discussed human genes in biomedical texts. CGVdb 1997 - 1998 data now online (Demonstrate Only).
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Chinese Gene Variation Database | cgvdb.tw Reviews

https://cgvdb.tw

The Chinese Gene Variation Database (CGVdb) is established to collect genetic mutations and other variations information in the Chinese population for clinical application and medical genetic research. Contents and structure of this ethnic mutation database follow the guidelines. Recommended by HUGO Human Genome Variation Society (HGVS). A natural language processing program for annotating the discussed human genes in biomedical texts. CGVdb 1997 - 1998 data now online (Demonstrate Only).

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1

Chinese Gene Variation Database

http://www.cgvdb.tw/about.php

The CGVdb obtains its source data by searching the PubMed database with our elaborately composed query string according to expert knowledge. The rudimentary document set fetched at the first step then undergoes a further manual verification to filter out false positives, and only those papers really concerning gene variations of the Chinese population are retained. Basic criteria for data selection are:. The reported cases with gene variation must come from the Chinese or its sub-ethnic group;. Database ...

2

Chinese Gene Variation Database

http://www.cgvdb.tw/help.php

Explaination for fields in the Search Result:. Gene name approved by HUGO HGNC. For details, see http:/ www.genenames.org/guidelines.html. Gene symbol approved by HUGO HGNC. For details, see http:/ www.genenames.org/guidelines.html. DNA variation following the notation recommended by HUGO Mutation Database Initiative (MDI). For details, see http:/ www.interscience.wiley.com/jpages/1059-7794/nomenclature.html. Reference sequence for that gene in NCBI s Nucleotide database under Entrez. Records the (sub)et...

3

Chinese Gene Variation Database

http://www.cgvdb.tw/statistics.php

Current CGV Report which have DNA Variation and/or A.A. Variation:. Current CGV Report which has A.A. Variation Only:. The Genes of current CGVdb content:. The Phenotypes of current CGVdb content:. The References of current CGVdb content:. CGVdb in progress Statistics. Variation Records which have been processed:. Variation Records processed to CGV Reports by merging same Variation from different References). Variation Records which under processing:. Current References which considered as CVRs:.

4

Chinese Gene Variation Database

http://www.cgvdb.tw/browse.php

This page is maintained by Prof. Kwang-Jen Hsiao. Inquiries about this page should be made to. Peitou P.O. Box 2-207, Taipei, Taiwan, 11216, R.O.C. Last update: Nov-06 2014.

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Introduction of HCC

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二 酗酒 肝癌最大的 禍首,除. 肝 癌好發年齡在 45 55 歲之間,尤以男性居多。 3、培養正確的醫療觀念 打針時不可 只換針頭、不換針筒 ,避免不必. 定期篩檢 大部份肝癌病人 血液中 甲型 胎. 蛋白 ( Alpha Fetoprotein ) 普遍會升. 10699 台北郵政 26-624 號信箱 電話 (02) 2703-6080 傳真 (02) 2703-6070. 19 May, 2014.

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門診表查詢網站

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為使民眾可透過網路,方便取得全國醫療機構之門診及掛號資訊,而於 85 年起建置 門診表查詢網站. 10699 台北郵政 26-624 號信箱. 31 Jul, 2013.

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Preventive Medicine Foundation

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周年暨 危急型先天心臟病篩檢 啟動記者會,臺北市自 98. 月起率先推出 新生兒聽力篩檢推廣計畫 ,新生兒在出生 24. 1 北市府推新生兒聽力篩檢3年有成 續推 新生兒危急型先天心臟病 篩檢,讓北市新生兒獲得更健全照護. 2 北市新生兒聽力篩檢計畫 守護新生兒健康 聽 [2013-09-17 自立晚報]. 3 新生兒聽力篩檢有成 北市續推先天心臟病篩檢 [2013-09-17 NOW NEWS今日新聞]. 10699 台北郵政 26-624 號信箱 電話 (02) 2703-6080 傳真 (02) 2703-6070. 13 May, 2014.

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Quality Assurance

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External Quality Assurance (EQA) for G6PD Newborn Screening Test. External Quality Assurance (EQA) for G6PD Quantitative Test in Taiwan. External Quality Assurance (EQA) for G6PD Quantitative Test in Philippines. 10699 台北郵政 26-624 號信箱 電話 (02) 2703-6080 傳真 (02) 2703-6070. 17 Jul, 2014.

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新生兒代謝異常疾病

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先天性德國麻疹症候群流行病學調查

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世界衛生組織 WHO )對於德國麻疹與 CRS的防治極為重視,分別針對疫苗施打與監視發表相關的標準及指引文獻。 美洲區署( AMRO / PAHO )於2010宣布已達到CRS消除,歐洲區署( EURO )則訂定以2015年消除CRS為目標。 依據 WHO發表之 德國麻疹與先天性德國麻疹症候群監偵指導原則及標準 ,要消除CRS除了維持常規疫苗高接種完成率達95%以上外,並要以完善的 疫情調查及實驗室診斷,來強化監視調查系統,提出有效的數據資料來證明消除成果。 本計畫透過蒐集分析國內外CRS相關文獻資料,了解國內外CRS的防治及監偵現況,同時進行回溯性調查,藉由檢閱聽損個案的去連結病歷,與利用 新生兒先天代謝異常疾病篩檢 的剩餘血片檢體進行德國麻疹 IgM抗體檢驗,進行國內CRS回溯性調查,並實證此檢測方法是可行也可靠的方法,未來將可應用於CRS回溯性及前瞻性的監視調查作業。 除此之外,亦委請全民健康保險研究資料庫 ( NHIRD )相關研究團隊協助設計CRS及相關病歷定義的組合搜尋條件,並進行資料庫搜尋及分析,搜尋出全國 IgM的檢驗數量,提供國內RubellaIgM的檢驗容量數據以供消除驗證使用。

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Preventive Medicine Foundation

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Preventive Medicine Foundation

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結核病防治與人權教育

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國立陽明大學教授 人權教育基金會執行長 周 碧 瑟. 最後,在此提供世界衛生組織公佈的簡易篩檢方法如下 咳嗽兩週( 2分 ),有痰( 2 分),體重減輕( 1分),沒有食慾( 1分),胸痛(1分 ),如果你有上述症狀達5分以上,建議你趕快就醫檢查。 若在台北市,可到台北市立聯合醫院和平院區 ( 聯絡人 徐慧芳護士,電話 2388-9595 分機2138. 或林森院區 ( 聯絡人 周艷秋護士,電話 2591-6680分機1122. 10699 台北郵政 26-624 號信箱 電話 (02) 2703-6080 傳真 (02) 2703-6070. 11 Sep, 2013.

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Chinese Gene Variation Database

The Chinese Gene Variation Database (CGVdb) is established to collect genetic mutations and other variations information in the Chinese population for clinical application and medical genetic research. Contents and structure of this ethnic mutation database follow the guidelines. Recommended by HUGO Human Genome Variation Society (HGVS). A natural language processing program for annotating the discussed human genes in biomedical texts. CGVdb 1997 - 1998 data now online (Demonstrate Only).

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