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2007 | 1 |
2012 | 1 |
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Recommendations for the diagnosis and management of childhood Prader-Willi syndrome in China.
Orphanet J Rare Dis. 2022 Jun 13;17(1):221. doi: 10.1186/s13023-022-02302-z.
Orphanet J Rare Dis. 2022.
PMID: 35698200
Free PMC article.
Review.
Kikuchi-Fujimoto disease manifesting as recurrent thrombocytopenia and Mobitz type II atrioventricular block in a 7-year-old girl: a case report and analysis of 138 Chinese childhood Kikuchi-Fujimoto cases with 10 years of follow-up in 97 patients.
Jun-Fen F, Chun-Lin W, Li L, Dayan C, Guan-Ping D, Fang H.
Jun-Fen F, et al. Among authors: chun lin w.
Acta Paediatr. 2007 Dec;96(12):1844-7. doi: 10.1111/j.1651-2227.2007.00523.x. Epub 2007 Oct 11.
Acta Paediatr. 2007.
PMID: 17931395
Review.
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Expression screening and annotation of Sepiella maindroni ink sac cDNA library.
Wei-Wei S, Chang-Kao M, Chu S, Yu-Yu Z, Ping-Ping Z, Chun-Lin W.
Wei-Wei S, et al. Among authors: chun lin w.
J Genet. 2012 Nov 28;91(3):e103-8.
J Genet. 2012.
PMID: 23257298
Free article.
No abstract available.
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