Multiplex-PCR is a useful and economical method to detect large exon deletions in severe hemophilia A in developing countries: Experience of Tunisia von Elmahmoudi, Hejer, JBALI, Chourouk, BESBES, Sawsen, BARRED, Rabeb, BELAKHAL, Rayhane, GOUIDER, Emna, ELMAHMOUDI, Hajer

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Coexistence of JAK2V617F and CALR mutation in Tunisian cohort with Philadelphia-negative chronic myeloproliferative neoplasms von Elmahmoudi, Hejer, Chourouk, Jbali, Wejden, Elborgi, Ons, Ghali, Kouther, Zahra, Emna, Gouider

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Factor VIII haplotypes frequencies in Tunisian hemophiliacs A von Elmahmoudi, Hejer, Belhedi, Nejla, Jlizi, Asma, Zahra, Kaouther, Meddeb, Balkis, Ben Ammar Elgaaied, Amel, Gouider, Emna

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First report of molecular diagnosis of Tunisian hemophiliacs A: identification of 8 novel causative mutations von Elmahmoudi, Hejer, Khodjet-el-khil, Houssein, Wigren, Edvard, Jlizi, Asma, Zahra, Kaouther, Pellechia, Dorothé, Vinciguerra, Christine, Meddeb, Balkis, Elggaaied, Amel Ben Ammar, Gouider, Emna

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Identification of genetic defects underlying FVII deficiency in 10 patients belonging to eight unrelated families of the North provinces from Tunisia von Elmahmoudi, Hejer, Ben-Lakhal, Fatma, Elborji, Wijden, Jlizi, Asma, Zahra, Kaouther, Sassi, Rim, Zorgan, Moez, Meddeb, Balkis, Elgaaied Ben Ammar, Amel, Gouider, Emna

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The Glanzmann's Thrombasthenia in Tunisia: A Cohort Study von Elmahmoudi, Hejer, Achour, Meriem, Belhedi, Nejla, Ben Neji, Hend, Zahra, Kaouther, Meddeb, Balkis, Gouider, Emna

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Identification of a novel mutation in the MCFD2 gene in a Tunisian family with combined factor V and VIII deficiency von Hejer, Elmahmoudi, Adnen, Laatiri Med, Asma, Jlizi, Ibtihel, Makhlouf, Benammar-Elgaaied, Amel, Gouider, Emna

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Structural analysis of two novel mutations in MCFD2 gene causing combined coagulation factors V and VIII deficiency von Abdallah, Hejer Elmahmoudi, Gouider, Emna, Stambouli, Nejla, Amor, Mohamed Ben, Jlizi, Asma, Belhedi, Nejla, Sassi, Rim, Khodjetelkhil, Houssein, Meddeb, Balkis, Hafsia, Raouf, Hamza, Adel, Elgaaied, Amel Benammar

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Identification of a novel mutation in the MCFD2 gene in a Tunisian family with combined factor V and VIII deficiency von Hejer, Elmahmoudi, Adnen, Laatiri Med, Asma, Jlizi, Ibtihel, Makhlouf, Benammar-Elgaaied, Amel, Gouider, Emna

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Structural analysis of two novel mutations in MCFD2 gene causing combined coagulation factors V and VIII deficiency von Abdallah, Hejer Elmahmoudi, Gouider, Emna, Stambouli, Nejla, Ben Amor, Mohamed, Jlizi, Asma, Belhedi, Nejla, Sassi, Rim, Khodjetelkhil, Houssein, Meddeb, Balkis, Hafsia, Raouf, Hamza, Adel, Elgaaied, Amel Benammar

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