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English Journal
- A Novel α2-Globin Gene Mutation: Hb Debao [α31(B12)Arg→Trp; HBA2: c.94A>T].
- Lin L1, Chen B1, Yi S1, Chen Q1, Wei H1, Li G2, Zheng C1, Qiu XX1, He S1.
- Hemoglobin.Hemoglobin.2017 Apr 2:1-3. doi: 10.1080/03630269.2017.1289102. [Epub ahead of print]
- PMID 28367658
- [Neonatal expression of beta-thalassemia trait associated with hereditary spherocytosis in two monozygotic twins].
- Ben Hamouda H1, Mahjoub B2, Soua H2, Laradi S3, Miled A3, Sfar MT2.
- Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.Arch Pediatr.2017 Feb;24(2):126-130. doi: 10.1016/j.arcped.2016.10.024. Epub 2016 Dec 12.
- PMID 27979672
- A Mouse Model for Human Unstable Hemoglobin Santa Ana.
- Miyashiro SI1, Massironi SM2, Mori CM3, Cruz CC2, Hagiwara MK1, Maiorka PC2.
- Comparative medicine.Comp Med.2016 Dec 1;66(6):437-444.
- PMID 28304246
Japanese Journal
- 栄養介入による男子大学生長距離ランナーの貧血指標の改善
- An Automated Hb A_2 Analyzer, HLC-723G7, for Diagnosis of β-Thalassemia
- 生後早期に遺伝子解析により診断されたヘモグロビンE症の1男児例
Related Pictures
★リンクテーブル★
[★]
- 英
- hypochromia、hypochromic
- 関
- 血色素減少、低色素血
[★]
- 英
- hypochromia
- 関
- 血色素減少、低色素
[★]
- 英
- hypochromia
- 関
- 低色素、低色素血
[★]
- 関
- hypochromia