基因剪切位點突變 (Chinese Wikipedia)

Analysis of information sources in references of the Wikipedia article "基因剪切位點突變" in Chinese language version.

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Jagiello, P; Hammans, C; Wieczorek, S; Arning, L; Stefanski, A; Strehl, H; Epplen, JT; Gencik, M. A novel splice site mutation in the TRIM37 gene causes mulibrey nanism in a Turkish family with phenotypic heterogeneity.. Human mutation. 2003-06, 21 (6): 630–5 [2020-02-01]. PMID 12754710. doi:10.1002/humu.10220. （原始内容存档于2020-02-01）.
Avela, K; Lipsanen-Nyman, M; Idänheimo, N; Seemanová, E; Rosengren, S; Mäkelä, TP; Perheentupa, J; Chapelle, AD; Lehesjoki, AE. Gene encoding a new RING-B-box-Coiled-coil protein is mutated in mulibrey nanism.. Nature genetics. 2000-07, 25 (3): 298–301 [2020-02-01]. PMID 10888877. doi:10.1038/77053. （原始内容存档于2020-02-01）.
Hämäläinen, RH; Mowat, D; Gabbett, MT; O'brien, TA; Kallijärvi, J; Lehesjoki, AE. Wilms' tumor and novel TRIM37 mutations in an Australian patient with mulibrey nanism.. Clinical genetics. 2006-12, 70 (6): 473–9 [2020-02-01]. PMID 17100991. doi:10.1111/j.1399-0004.2006.00700.x. （原始内容存档于2020-02-01）.

Berget, Susan. Exon Recognition in Vertebrate Splicing. The Journal of Biological Chemistry. [2019-01-23]. （原始内容存档于2020-03-01）.

Jagiello, P; Hammans, C; Wieczorek, S; Arning, L; Stefanski, A; Strehl, H; Epplen, JT; Gencik, M. A novel splice site mutation in the TRIM37 gene causes mulibrey nanism in a Turkish family with phenotypic heterogeneity.. Human mutation. 2003-06, 21 (6): 630–5 [2020-02-01]. PMID 12754710. doi:10.1002/humu.10220. （原始内容存档于2020-02-01）.
Avela, K; Lipsanen-Nyman, M; Idänheimo, N; Seemanová, E; Rosengren, S; Mäkelä, TP; Perheentupa, J; Chapelle, AD; Lehesjoki, AE. Gene encoding a new RING-B-box-Coiled-coil protein is mutated in mulibrey nanism.. Nature genetics. 2000-07, 25 (3): 298–301 [2020-02-01]. PMID 10888877. doi:10.1038/77053. （原始内容存档于2020-02-01）.
Hämäläinen, RH; Mowat, D; Gabbett, MT; O'brien, TA; Kallijärvi, J; Lehesjoki, AE. Wilms' tumor and novel TRIM37 mutations in an Australian patient with mulibrey nanism.. Clinical genetics. 2006-12, 70 (6): 473–9 [2020-02-01]. PMID 17100991. doi:10.1111/j.1399-0004.2006.00700.x. （原始内容存档于2020-02-01）.

Jagiello, P; Hammans, C; Wieczorek, S; Arning, L; Stefanski, A; Strehl, H; Epplen, JT; Gencik, M. A novel splice site mutation in the TRIM37 gene causes mulibrey nanism in a Turkish family with phenotypic heterogeneity.. Human mutation. 2003-06, 21 (6): 630–5 [2020-02-01]. PMID 12754710. doi:10.1002/humu.10220. （原始内容存档于2020-02-01）.
Avela, K; Lipsanen-Nyman, M; Idänheimo, N; Seemanová, E; Rosengren, S; Mäkelä, TP; Perheentupa, J; Chapelle, AD; Lehesjoki, AE. Gene encoding a new RING-B-box-Coiled-coil protein is mutated in mulibrey nanism.. Nature genetics. 2000-07, 25 (3): 298–301 [2020-02-01]. PMID 10888877. doi:10.1038/77053. （原始内容存档于2020-02-01）.
Hämäläinen, RH; Mowat, D; Gabbett, MT; O'brien, TA; Kallijärvi, J; Lehesjoki, AE. Wilms' tumor and novel TRIM37 mutations in an Australian patient with mulibrey nanism.. Clinical genetics. 2006-12, 70 (6): 473–9 [2020-02-01]. PMID 17100991. doi:10.1111/j.1399-0004.2006.00700.x. （原始内容存档于2020-02-01）.

Understanding Cancer Genomics: Splice Site Mutations. National Cancer Institute. [2019-01-25]. （原始内容存档于2020-02-03）.

Berget, Susan. Exon Recognition in Vertebrate Splicing. The Journal of Biological Chemistry. [2019-01-23]. （原始内容存档于2020-03-01）.
Understanding Cancer Genomics: Splice Site Mutations. National Cancer Institute. [2019-01-25]. （原始内容存档于2020-02-03）.
Jagiello, P; Hammans, C; Wieczorek, S; Arning, L; Stefanski, A; Strehl, H; Epplen, JT; Gencik, M. A novel splice site mutation in the TRIM37 gene causes mulibrey nanism in a Turkish family with phenotypic heterogeneity.. Human mutation. 2003-06, 21 (6): 630–5 [2020-02-01]. PMID 12754710. doi:10.1002/humu.10220. （原始内容存档于2020-02-01）.
Avela, K; Lipsanen-Nyman, M; Idänheimo, N; Seemanová, E; Rosengren, S; Mäkelä, TP; Perheentupa, J; Chapelle, AD; Lehesjoki, AE. Gene encoding a new RING-B-box-Coiled-coil protein is mutated in mulibrey nanism.. Nature genetics. 2000-07, 25 (3): 298–301 [2020-02-01]. PMID 10888877. doi:10.1038/77053. （原始内容存档于2020-02-01）.
Hämäläinen, RH; Mowat, D; Gabbett, MT; O'brien, TA; Kallijärvi, J; Lehesjoki, AE. Wilms' tumor and novel TRIM37 mutations in an Australian patient with mulibrey nanism.. Clinical genetics. 2006-12, 70 (6): 473–9 [2020-02-01]. PMID 17100991. doi:10.1111/j.1399-0004.2006.00700.x. （原始内容存档于2020-02-01）.