Warfare and children
- 作者Frank Shann
- 卷第46卷
- 期第5期
- 印刷ISSN1034-4810
- 电子ISSN1440-1754
- 文件大小402.26KB
- 发表时间2010
- DOI10.1111/j.1440-1754.2009.01673.x
- 页码217-221
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Handbook of PaediatricsArchives of Disease in Childhood · 1955
Handbook of PaediatricsBarbor, P R H · Archives of Disease in Childhood · 1989
Book Review: New Editions: Handbook of PaediatricsScottish Medical Journal · 1966
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