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Hb Taybe (alpha 38 or 39 THR deleted): an alpha-globin defect, silent in the heterozygous state and producing severe hemolytic anemia in the homozygous. [electronic resource] by
- Galacteros, F
- Girodon, E
- M'Rad, A
- Martin, J
- Goossens, M
- Jaber, L
- Cohen, I J
- Tamary, H
- Goshen, Y
- Zaizov, R
Producer: 19950119
In:
Comptes rendus de l'Academie des sciences. Serie III, Sciences de la vie vol. 317
Availability: No items available.
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26.
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Hb Saint Nazaire (beta 103[G5]Phe-->Ile): a new example of polycythemia due to a hemoglobin variant with increased oxygen affinity. [electronic resource] by
- Wajcman, H
- Kister, J
- M'Rad, A
- Promé, D
- Milpied, N
- Rapp, M J
- Harousseau, J L
- Riou, J
- Bardakdjian, J
- Galacteros, F
Producer: 19930901
In:
American journal of hematology vol. 44
Availability: No items available.
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