框移突變 (Chinese Wikipedia)

Analysis of information sources in references of the Wikipedia article "框移突變" in Chinese language version.

refsWebsite

Global rank Chinese rank

1^st place

4^th place

5^th place

2^nd place

23^rd place

234^th place

227^th place

459^th place

752^nd place

102^nd place

492^nd place

1,684^th place

696^th place

cancer.gov

Cancer Genomics. National Cancer Institute at the National Institute of Health. [2013-03-24]. （原始内容存档于2013-03-18）.

Myerowitz, R. Tay-Sachs disease-causing mutations and neutral polymorphisms in the Hex A gene.. Human Mutation. 1997, 9 (3): 195–208. PMID 9090523. doi:10.1002/(SICI)1098-1004(1997)9:3<195::AID-HUMU1>3.0.CO;2-7.
Rader DJ, Cohen J, Hobbs HH. Monogenic hypercholesterolemia: new insights in pathogenesis and treatment.. J Clin Invest. 2003, 111 (12): 1795–803. PMC 161432 . PMID 12813012. doi:10.1172/JCI18925.
Ogura Y, Bonen DK, Inohara N, Nicolae DL, Chen FF, Ramos R, Britton H, Moran T, Karaliuskas R, Duerr RH, Achkar JP, Brant SR, Bayless TM, Kirschner BS, Hanauer SB, Nuñez G, Cho JH. A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease. (PDF). Nature. 2001-05-31, 411 (6837): 603–6 [2021-04-22]. PMID 11385577. doi:10.1038/35079114. hdl:2027.42/62856. （原始内容存档 (PDF)于2020-06-02）.

Ogura Y, Bonen DK, Inohara N, Nicolae DL, Chen FF, Ramos R, Britton H, Moran T, Karaliuskas R, Duerr RH, Achkar JP, Brant SR, Bayless TM, Kirschner BS, Hanauer SB, Nuñez G, Cho JH. A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease. (PDF). Nature. 2001-05-31, 411 (6837): 603–6 [2021-04-22]. PMID 11385577. doi:10.1038/35079114. hdl:2027.42/62856. （原始内容存档 (PDF)于2020-06-02）.

Myerowitz, R. Tay-Sachs disease-causing mutations and neutral polymorphisms in the Hex A gene.. Human Mutation. 1997, 9 (3): 195–208. PMID 9090523. doi:10.1002/(SICI)1098-1004(1997)9:3<195::AID-HUMU1>3.0.CO;2-7.
Rader DJ, Cohen J, Hobbs HH. Monogenic hypercholesterolemia: new insights in pathogenesis and treatment.. J Clin Invest. 2003, 111 (12): 1795–803. PMC 161432 . PMID 12813012. doi:10.1172/JCI18925.
Ogura Y, Bonen DK, Inohara N, Nicolae DL, Chen FF, Ramos R, Britton H, Moran T, Karaliuskas R, Duerr RH, Achkar JP, Brant SR, Bayless TM, Kirschner BS, Hanauer SB, Nuñez G, Cho JH. A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease. (PDF). Nature. 2001-05-31, 411 (6837): 603–6 [2021-04-22]. PMID 11385577. doi:10.1038/35079114. hdl:2027.42/62856. （原始内容存档 (PDF)于2020-06-02）.

Ogura Y, Bonen DK, Inohara N, Nicolae DL, Chen FF, Ramos R, Britton H, Moran T, Karaliuskas R, Duerr RH, Achkar JP, Brant SR, Bayless TM, Kirschner BS, Hanauer SB, Nuñez G, Cho JH. A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease. (PDF). Nature. 2001-05-31, 411 (6837): 603–6 [2021-04-22]. PMID 11385577. doi:10.1038/35079114. hdl:2027.42/62856. （原始内容存档 (PDF)于2020-06-02）.

DNA Is Constantly Changing through the Process of Mutation. Nature. [2019-05-17]. （原始内容存档于2021-08-03）.
Ogura Y, Bonen DK, Inohara N, Nicolae DL, Chen FF, Ramos R, Britton H, Moran T, Karaliuskas R, Duerr RH, Achkar JP, Brant SR, Bayless TM, Kirschner BS, Hanauer SB, Nuñez G, Cho JH. A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease. (PDF). Nature. 2001-05-31, 411 (6837): 603–6 [2021-04-22]. PMID 11385577. doi:10.1038/35079114. hdl:2027.42/62856. （原始内容存档 (PDF)于2020-06-02）.
Cancer Genomics. National Cancer Institute at the National Institute of Health. [2013-03-24]. （原始内容存档于2013-03-18）.