Two familial cases of Hb Tyne confirm instability as cause of low expression.
- Published in:
- Thalassemia Reports, 2017, v. 7, n. 1, p. 8, doi. 10.4081/thal.2017.6504
- By:
- Publication type:
- Article
Works matching IS 20394357 AND DT 2017 AND VI 7 AND IP 1
Results: 7
1
2
Granulocyte-colony stimulating factor plus plerixafor in patients with β-thalassemia major results in the effective mobilization of primitive CD34+ cells with specific gene expression profile.
- Published in:
- Thalassemia Reports, 2017, v. 7, n. 1, p. 11, doi. 10.4081/thal.2017.6392
- By:
- Publication type:
- Article
3
Fertility assessment in thalassemic men.
- Published in:
- Thalassemia Reports, 2017, v. 7, n. 1, p. 21, doi. 10.4081/thal.2017.6362
- By:
- Publication type:
- Article
4
Spectrum of types of thalassemias and hemoglobinopathies: study in a tertiary level children hospital in Bangladesh.
- Published in:
- Thalassemia Reports, 2017, v. 7, n. 1, p. 18, doi. 10.4081/thal.2017.6354
- By:
- Publication type:
- Article
5
No transfusion is the best transfusion: a rare case.
- Published in:
- 2017
- By:
- Publication type:
- Case Study
6
Incidental detection of a rare hemoglobin variant (Hemoglobin N Seattle) leading to undetectable levels of HbA1c in a diabetic female: a case report.
- Published in:
- 2017
- By:
- Publication type:
- Case Study
7
Alpha hemoglobinophaties in Rosario, Argentina.
- Published in:
- Thalassemia Reports, 2017, v. 7, n. 1, p. 3, doi. 10.4081/thal.2017.5655
- By:
- Publication type:
- Article