Array‐CGH study of partial trisomy 9p without mental retardation von Abdallah Bouhjar, Inesse Ben, Hannachi, Hanane, Mougou Zerelli, Soumaya, Labalme, Audrey, Gmidène, Abir, Soyah, Najla, Missaoui, Sonia, Sanlaville, Damien, Elghezal, Hatem, Saad, Ali

Volltext

Cytogenetic profile of a large cohort of Tunisian de novo acute myeloid leukemia von Gmidène, Abir, Sennana, Hlima, Wahchi, Ines, Youssef, Yosra Ben, Jeddi, Ramzi, Elloumi, Moez, Saad, Ali

Volltext

T(1;21;8)(p34;q22;q22): a novel variant of t(8;21) in acute myeloblastic leukemia with maturation von Gmidène, Abir, Frikha, Rim, Sennana, Hlima, Elghezal, Hatem, Elloumi, Moez, Saad, Ali

Volltext

Chromosomal microarray analysis of functional Xq27-qter disomy and deletion 3p26.3 in a boy with Prader–Willi like features and hypotonia von Ben-Abdallah-Bouhjar, Inesse, Hannachi, Hanene, Labalme, Audrey, Gmidène, Abir, Mougou, Soumaya, Soyah, Najla, Gribaa, Moez, Sanlaville, Damien, Elghezal, Hatem, Saad, Ali

Volltext

An unusual three-way translocation t(21;8;1)(q22;q22;q32) in a case of acute myeloid leukemia (M2) von GMIDENE, Abir, SENNANA, Hlima, FRIKHA, Rim, ELLOUMI, Moez, BELAAJ, Hatem, SAAD, Ali

Volltext

Multiple myeloma following essential thrombocythemia von YOSRA BEN YOUSSEF, GMIDENE, Abir, BOUABID, Zahreddine, BOUALLEGUI, Sonia, SRIHA, Badreddine, ZAIER, Monia, SENNANA, Hlima, KHELIF, Abserrahim

Volltext

Cytogenetic abnormalities in Tunisian de novo myelodysplastic syndrome: A comparison with other populations von Gmidène, Abir, Sennana, Hlima, Fenaux, Pierre, Laatiri, Adnène, Zarrouk, Mohamed, Bouaziz, Houssem, Harrabi, Imed, Saad, Ali

Volltext

Molecular cytogenetic and phenotypic characterization of ring chromosome 13 in three unrelated patients von Abdallah-Bouhjar, Inesse B., Mougou-Zerelli, Soumaya, Hannachi, Hanene, Gmidène, Abir, Labalme, Audrey, Soyah, Najla, Sanlaville, Damien, Saad, Ali, Elghezal, Hatem

Volltext

Cytogenetic analysis of 298 newly diagnosed cases of acute lymphoblastic leukaemia in Tunisia von Gmidène, Abir, Sennana, Hlima, Elghezal, Hatem, Ziraoui, Sihem, Youssef, Yosra Ben, Elloumi, Moez, Issaoui, Lamia, Harrabi, Imed, Raynaud, Sophie, Saad, Ali

Volltext

ETV6-RUNX1 Rearrangement in Tunisian Pediatric B-Lineage Acute Lymphoblastic Leukemia von Gmidène, Abir, Elghezal, Hatem, Sennana, Hlima, Ben Youssef, Yosra, Meddeb, Balkiss, Elloumi, Moez, Khlif, Abderrahim, Saad, Ali

Volltext

Trisomy and tetrasomy 15q11-q13 diagnosed by molecular cytogenetic analysis in two patients with mental retardation von Bouhjar, Inesse Ben Abdallah, Gmidène, Abir, Soyah, Najla, Hanene, Hannachi, Mougou, Soumaya, Elghezal, Hatem, Saad, Ali

Volltext

Cytogenetic analysis in a large series of children with non-syndromic mental retardation von Bouhjar, Inesse Ben Abdallah, Gmidène, Abir, Mougou-Zrelli, Soumaya, Hannachi, Hanene, Soyah, Najla, Gadour, Naoufel, Harrabi, Imed, Elghezal, Hatem, Saad, Ali

Volltext

New Variant Translocation (8;9;21)(q22;p24;q22) in a Patient with Granulocytic Sarcoma Concurrent with Acute Myeloid Leukemia von Abir, Gmidène, Ines, Wahchi, Sondes, Meksi, Ramzi, Jeddi, Balkis, Meddeb, Ali, Saad, Hlima, Sennana

Volltext

CD4+/CD56+ Hematodermic Neoplasm Presenting in the Skin: A Tunisian Case Report and Current Review of the Literature von Youssef, Yosra Ben, Sayed, Nessrine Ben, Zahra, Kmira, Gmidène, Abir, Salah, Naouel Ben, Abdelkader, Atef Ben, Brahem, Nejia, Sennana, Hlima, Belajouza, Colanda, Khelif, Abderrahim

Volltext

Molecular cytogenetic and phenotypic characterization of ring chromosome 13 in three unrelated patients von Abdallah-Bouhjar, Inesse B, Mougou-Zerelli, Soumaya, Hannachi, Hanene, Gmidène, Abir, Labalme, Audrey, Soyah, Najla, Sanlaville, Damien, Saad, Ali, Elghezal, Hatem

Volltext

Array-CGH study of partial trisomy 9p without mental retardation von Abdallah Bouhjar, Inesse Ben, Hannachi, Hanane, Mougou Zerelli, Soumaya, Labalme, Audrey, Gmidène, Abir, Soyah, Najla, Missaoui, Sonia, Sanlaville, Damien, Elghezal, Hatem, Saad, Ali

Volltext