腺苷脱氨酶缺乏症 (Chinese Wikipedia)
Analysis of information sources in references of the Wikipedia article "腺苷脱氨酶缺乏症" in Chinese language version.
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archive.org
- Arredondo-Vega FX, Santisteban I, Daniels S, Toutain S, Hershfield MS. Adenosine deaminase deficiency: genotype-phenotype correlations based on expressed activity of 29 mutant alleles. American Journal of Human Genetics. October 1998, 63 (4): 1049–59. PMC 1377486
. PMID 9758612. doi:10.1086/302054.
doi.org
- Hirschhorn R, Vawter GF, Kirkpatrick JA Jr, Rosen FS. Adenosine deaminase deficiency: frequency and comparative pathology in autosomally recessive severe combined immunodeficiency. Clinical Immunology and Immunopathology. September 1979, 14 (1): 107–20. PMID 477037. doi:10.1016/0090-1229(79)90131-4.
- Hershfield MS. Genotype is an important determinant of phenotype in adenosine deaminase deficiency. Current Opinion in Immunology. October 2003, 15 (5): 571–7. PMID 14499267. doi:10.1016/S0952-7915(03)00104-3.
- Arredondo-Vega FX, Santisteban I, Daniels S, Toutain S, Hershfield MS. Adenosine deaminase deficiency: genotype-phenotype correlations based on expressed activity of 29 mutant alleles. American Journal of Human Genetics. October 1998, 63 (4): 1049–59. PMC 1377486 . PMID 9758612. doi:10.1086/302054.
kepu.net.cn
- DNA-生命的螺旋博物館＿中國科普博覽. www.kepu.net.cn. [2019-08-27]. （原始内容存档于2019-08-27）.
nih.gov
ncbi.nlm.nih.gov
- Hirschhorn R, Vawter GF, Kirkpatrick JA Jr, Rosen FS. Adenosine deaminase deficiency: frequency and comparative pathology in autosomally recessive severe combined immunodeficiency. Clinical Immunology and Immunopathology. September 1979, 14 (1): 107–20. PMID 477037. doi:10.1016/0090-1229(79)90131-4.
- Hershfield MS. Genotype is an important determinant of phenotype in adenosine deaminase deficiency. Current Opinion in Immunology. October 2003, 15 (5): 571–7. PMID 14499267. doi:10.1016/S0952-7915(03)00104-3.
- Arredondo-Vega FX, Santisteban I, Daniels S, Toutain S, Hershfield MS. Adenosine deaminase deficiency: genotype-phenotype correlations based on expressed activity of 29 mutant alleles. American Journal of Human Genetics. October 1998, 63 (4): 1049–59. PMC 1377486 . PMID 9758612. doi:10.1086/302054.
ghr.nlm.nih.gov
- Adenosine deaminase deficiency. 美國國家醫學圖書館. [2019-08-22]. （原始内容存档于2020-08-07） （英语）.
nytimes.com
- Glaser, Vicki. Eloise R. Giblett, Blood Research Leader, Dies at 88. The New York Times. 2009-09-23 [2019-08-23]. （原始内容存档于2021-01-13） （英语）.
- Naam, Ramez. 'More Than Human' - New York Times. The New York Times. 2005-07-03 [2008-02-28]. （原始内容存档于2015-05-26）.
web.archive.org
- Adenosine deaminase deficiency. 美國國家醫學圖書館. [2019-08-22]. （原始内容存档于2020-08-07） （英语）.
- Glaser, Vicki. Eloise R. Giblett, Blood Research Leader, Dies at 88. The New York Times. 2009-09-23 [2019-08-23]. （原始内容存档于2021-01-13） （英语）.
- UpToDate. www.uptodate.com. [2019-08-27]. （原始内容存档于2021-03-21） （英语）.
- Naam, Ramez. 'More Than Human' - New York Times. The New York Times. 2005-07-03 [2008-02-28]. （原始内容存档于2015-05-26）.
- DNA-生命的螺旋博物館＿中國科普博覽. www.kepu.net.cn. [2019-08-27]. （原始内容存档于2019-08-27）.