Search Results - Romdhane, Samira Ibala

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  1. 1
    A new mutation identified in SPATA16 in two globozoospermic patients

    A new mutation identified in SPATA16 in two globozoospermic patients by ElInati, Elias, Fossard, Camille, Okutman, Ozlem, Ghédir, Houda, Ibala-Romdhane, Samira, Ray, Pierre F., Saad, Ali, Hennebicq, Sylvianne, Viville, Stéphane

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  2. 2
    Nuclear sperm integrity and ICSI prognosis in Tunisian patients with MMAF syndrome (multiple morphological abnormalities of the sperm flagella)

    Nuclear sperm integrity and ICSI prognosis in Tunisian patients with MMAF syndrome (multiple morphological abnormalities of the sperm flagella) by Braham, Asma, Ghedir, Houda, Ben Khedher, Myriam Beya, Ajina, Mounir, Saad, Ali, Ibala-Romdhane, Samira

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  3. 3
    Identification of a new DPY19L2 mutation and a better definition of DPY19L2 deletion breakpoints leading to globozoospermia

    Identification of a new DPY19L2 mutation and a better definition of DPY19L2 deletion breakpoints leading to globozoospermia by Ghédir, Houda, Ibala-Romdhane, Samira, Okutman, Ozlem, Viot, Géraldine, Saad, Ali, Viville, Stéphane

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  4. 4
    Analysis of H19 methylation in control and abnormal human embryos, sperm and oocytes

    Analysis of H19 methylation in control and abnormal human embryos, sperm and oocytes by Ibala-Romdhane, Samira, Al-Khtib, Mohamed, Khoueiry, Rita, Blachère, Thierry, Guérin, Jean-François, Lefèvre, Annick

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  5. 5
    Macrozoospermia: screening for the homozygous c.144delC mutation in AURKC gene in infertile men and estimation of its heterozygosity frequency in the Tunisian population

    Macrozoospermia: screening for the homozygous c.144delC mutation in AURKC gene in infertile men and estimation of its heterozygosity frequency in the Tunisian population by Ghédir, Houda, Gribaa, Moez, Mamaî, Ons, Ben Charfeddine, Ilhem, Braham, Asma, Amara, Abdelbasset, Mehdi, Meriem, Saad, Ali, Ibala-Romdhane, Samira

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  6. 6
    Abnormal methylation of KCNQ1OT1 and differential methylation of H19 imprinting control regions in human ICSI embryos

    Abnormal methylation of KCNQ1OT1 and differential methylation of H19 imprinting control regions in human ICSI embryos by Khoueiry, Rita, Ibala-Romdhane, Samira, Al-Khtib, Mohamed, Blachère, Thierry, Lornage, Jacqueline, Guérin, Jean-.François, Lefèvre, Annick

    Published in Zygote (Cambridge)
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  7. 7
    Large duplication 4q25–q34 with mild clinical effect

    Large duplication 4q25–q34 with mild clinical effect by Elghezal, Hatem, Sendi, Halima Sennana, Monastiri, Kamel, Lapierre, Jean Michel, Romdhane, Samira Ibala, Mougou, Soumaya, Saad, Ali

    Published in Annales de génétique
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