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Fibrinogen Mahdia: A congenitally abnormal fibrinogen characterized by defective fibrin polymerization. [electronic resource] by
- Amri, Y
- Jouini, H
- Becheur, M
- Dabboubi, R
- Mahjoub, B
- Messaoud, T
- Sfar, M T
- Casini, A
- de Moerloose, P
- Toumi, N E H
Producer: 20180319
In:
Haemophilia : the official journal of the World Federation of Hemophilia vol. 23
Availability: No items available.
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5.
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Glucose-6-phosphate dehydrogenase deficiency in Tunisia: molecular data and phenotype-genotype association. [electronic resource] by
- Laouini, N
- Bibi, A
- Ammar, H
- Kazdaghli, K
- Ouali, F
- Othmani, R
- Amdouni, S
- Haloui, S
- Sahli, C A
- Jouini, L
- Hadj Fredj, S
- Siala, H
- Ben Romdhane, N
- Toumi, N E
- Fattoum, S
- Messsaoud, T
Producer: 20130617
In:
Molecular biology reports vol. 40
Availability: No items available.
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6.
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Association between clinical expression and molecular heterogeneity in β-thalassemia Tunisian patients. [electronic resource] by
- Jouini, L
- Sahli, C A
- Laaouini, N
- Ouali, F
- Ben Youssef, I
- Dakhlaoui, B
- Othmeni, R
- Ouennich, F
- Hadj Fredj, S
- Siala, H
- Becher, M
- Toumi, N E
- Fattoum, S
- Hafsia, R
- Bibi, A
- Messaoud, T
Producer: 20140611
In:
Molecular biology reports vol. 40
Availability: No items available.
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