Familial Autism Spectrum Disorder : A clinical study from South Tunisia von Boujelben, I., Chaabane, M., Ben ayed, I., Ben Touhemi, D., Gharbi, N., Guirat, M., HajKacem, I., Ayadi, H., Kamoun, H., Moalla, Y.

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Psychological impact of motor impairment in tow forms of congenital muscular dystrophy von Boujelbene, I., Chaabane, M., Guirat, M., Ben Touhemi, D., Gharbi, N., Yousr, M., Kamoun, H., Ben Ayed, I.

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The psychological impact on parents of children with pyridoxine-dependent epilepsy von Boujelbene, I., Chaabane, M., Guirat, M., Ben Touhemi, D., Guidara, S., Moalla, Y., Kamoun, H., Ben Ayed, I.

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Neuropsychiatric manifestations in Cornelia de Lange syndrome von Majdoub, F, Souissi, A, Trabelsi, M, Ziadi, A, Belguith, N, Maazoul, F, Guirat, M, Boujelbene, I, Kamoun, H, Mrad, R, Masmoudi, S, I Ben Ayed

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Mutational analysis of JAK2V617F in tunisian polycythemia vera patients von Frikha, R., Elloumi, M., Kamoun, H.

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Transforming part-sequencing problems in a robotic cell into a GTSP von Zahrouni, W, Kamoun, H

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Chromosomal instability associated with a novel BLM frameshift mutation (c.1980-1982delAA) in two unrelated Tunisian families with Bloom syndrome von Salah, G. Ben, Salem, I. Hadj, Masmoudi, A., Rhouma, B. Ben, Turki, H., Fakhfakh, F., Ayadi, H., Kamoun, H.

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Phenotypic variability in a Tunisian family with X-linked adrenoleukodystrophy caused by the p.Gln316Pro novel mutation von Kallabi, F., Dr, Ellouz, E., Dr, Kaabechi, N., Pr, Keskes, L., Pr, Triki, C., Pr, Kamoun, H., Pr

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PP-73 - Discontinuation of tyrosine kinase inhibitors in chronic myeloid leukemia: a single-center experience von Frikha, R., Elloumi, M., Kamoun, H.

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Discontinuation of tyrosine kinase inhibitors in chronic myeloid leukemia: a single-center experience von Frikha, R., Elloumi, M., Kamoun, H.

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A novel mutation MT-COIII m.9267G>C and MT-COI m.5913G>A mutation in mitochondrial genes in a Tunisian family with maternally inherited diabetes and deafness (MIDD) associated with... von Tabebi, M, Mkaouar-Rebai, E., Dr, Mnif, M., Dr, Kallabi, F, Ben Mahmoud, A, Ben Saad, W., Dr, Charfi, N., Dr, Keskes-Ammar, L., Pr, Kamoun, H., Pr, Abid, M., Pr, Fakhfakh, F., Pr

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PP-75 - Lack of association between MTHFR C677T and risk of chronic myeloid leukemia von Jemaa, M. Ben, Turki, F., Kamoun, H., Frikha, R.

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Lack of association between MTHFR C677T and risk of chronic myeloid leukemia von Jemaa, M. Ben, Turki, F., Kamoun, H., Frikha, R.

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Chediak–Higashi syndrome presenting in accelerated phase: A case report and literature review von Maaloul, I, Talmoudi, J, Chabchoub, I, Ayadi, L, Kamoun, T.H, Boudawara, T, Kallel, C.H, Hachicha, M

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TCF7L2 is associated with type 2 diabetes in nonobese individuals from Tunisia von Bouhaha, R., Choquet, H., Meyre, D., Abid Kamoun, H., Ennafaa, H., Baroudi, T., Sassi, R., Vaxillaire, M., Elgaaied, A., Froguel, P., Cauchi, S.

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Effet fondateur et estimation de l’âge de la mutation fondatrice dans trois pays maghrébins : à propos de 66 patients atteints du syndrome d’Allgrove von Kallabi, F, Tebaibia, A, Boudjella, L, Mahfoudh, N, Kamoun, A, Gaddour, L, Amoura, S, Bouali- Benhalima, M, Winbo, A, Keskes, L, Kamoun, H

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Étude génétique du Syndrome d’Allgrove dans la région du Maghreb : histoire de mutation majoritaire et effet fondateur von Kallabi, F, Boudjella, L, Tebaibia, A, Kamoun, H

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Les anomalies de la différenciation sexuelle 46, XY : diagnostic moléculaire chez 14 femmes Tunisiennes von Ben Rhouma, B, Fakhfakh, F, Abdelhedi, F, Kamoun, T, Mnif, M, Hachicha, M, Kamoun, H, Keskes, L, Belguith, N

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PB1921 COMPREHENSIVE ANALYSIS OF MOLECULAR RESPONSE IN TUNISIAN CML PATIENTS FOR TREATMENT DISCONTINUATION von Frikha, R., Elloumi, M., Kamoun, H.

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La déficience en enzyme HSD17B3 n’est plus une rare étiologie des 46, XY DSD dans la population tunisienne von Ben Rhouma, B, Engeli, R, Fakhfakh, F., Pr, Mnif, M., Pr, Kamoun, T., Pr, Odermatt, A., Pr, Kamoun, H., Pr, Keskes, L., Pr, Belguith, N., Dr

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