Found: 5
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Partial tandem duplication of MLL gene in acute myeloid leukemia with translocation (11;17)(q23;q12–21).
- Published in:
- American Journal of Hematology, 2005, v. 80, n. 1, p. 46, doi. 10.1002/ajh.20411
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- Publication type:
- Article
A Case of Sporadic Blau Syndrome with an Uncommon Clinical Course.
- Published in:
- Case Reports in Rheumatology, 2018, p. 1, doi. 10.1155/2018/6292308
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- Publication type:
- Article
Mutations of syntaxin 11 and SNAP23 genes as causes of familial hemophagocytic lymphohistiocytosis were not found in Japanese people.
- Published in:
- Journal of Human Genetics, 2005, v. 50, n. 11, p. 600, doi. 10.1007/s10038-005-0293-1
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- Publication type:
- Article
High-dose Cepharanthin for pediatric chronic immune thrombocytopenia in Japan.
- Published in:
- Pediatrics International, 2017, v. 59, n. 3, p. 303, doi. 10.1111/ped.13151
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- Publication type:
- Article
Nasal hemophilic pseudotumor in a patient with mild hemophilia A and allergic rhinitis.
- Published in:
- Pediatrics International, 2017, v. 59, n. 2, p. 237, doi. 10.1111/ped.13197
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- Publication type:
- Article