Genetics and cytogenetics

Néjia Braham-Jmili, Linda Khefacha, Yosra Ben Youssef, Ibtihel Ellouze, Halima Sendi Sennana, Monder Kortas

5q- syndrome: Experience of Farhat Hached hospital of Sousse

https://doi.org/10.71699/revtunbiolclin.v23i1.90

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DOI: https://doi.org/10.71699/revtunbiolclin.v23i1.90

Asma Bouassida, Sarra Salem Fekih, Wejden El Borgi, Fatma Ben Lakhal, Hend Ben Neji, Balkiss Meddeb, Emna Gouider

Acute myeloid leukemia cup-like nuclei: About a case and literature review

https://doi.org/10.71699/revtunbiolclin.v28i2.135

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DOI: https://doi.org/10.71699/revtunbiolclin.v28i2.135

Ahlem Sahli , Sondess Hadj Fredj , Chaima Sahli , Rym Dabboubi , Hajer Siala , Taïeb Ben Messaoud

Biochemical and molecular study in Tunisian cystic fibrosis population

https://doi.org/10.71699/revtunbiolclin.v25i1.101

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DOI: https://doi.org/10.71699/revtunbiolclin.v25i1.101

Ahlem Sahli, Faida Ouali, Rym Dabboubi, Sondess Hadj Fredj, Nabila Meddeb, Naila Mzoughi, Taieb Messaoud

Biological particularities of sickle cell syndrome

https://doi.org/10.71699/revtunbiolclin.v28i2.133

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DOI: https://doi.org/10.71699/revtunbiolclin.v28i2.133

Wided Maatamri, Haifa Regaieg, Amira Braham, Halima Sendi, Yosra Ben Youssef, Néjia Braham Jmili, Mondher Kortas

Clinico-biological and therapeutic features of promyelocytic acute leukemias: about 43 cases

https://doi.org/10.71699/revtunbiolclin.v28i2.134

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DOI: https://doi.org/10.71699/revtunbiolclin.v28i2.134

Fehmi Nasrallah, Mohamed B. Hammami, Sameh Hadj Taieb, Haifa Sanhaji, Moncef Feki

Early and fortuitous diagnosis of alkaptonuria while searching other inherited metabolic diseases. Three cases report.

https://doi.org/10.71699/revtunbiolclin.v22i1.84

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DOI: https://doi.org/10.71699/revtunbiolclin.v22i1.84

S. FATTOUM, A. BIBI, H. SIALA, T. MESSAOUD

echniques and strategy for identifying molecular defects in hemoglobinopathies in Tunisia

https://doi.org/10.71699/revtunbiolclin.vi19.230

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DOI: https://doi.org/10.71699/revtunbiolclin.vi19.230

Néjia Braham-Jmili , Mohamed Becha , Béchir Achour , Rihem Mezrigui , Yosra Ben youssef , Halima Sendi-Sennana , Ali Saad , Abderrahim Khelif , Mondher Kortas

Evolution in the diagnosis of myelodysplastic syndromes: Experience of Farhat Hached hospital

https://doi.org/10.71699/revtunbiolclin.v26i2.109

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DOI: https://doi.org/10.71699/revtunbiolclin.v26i2.109

Chaïma Sahli, Sondess Hadj Fredj, Taieb Messaoud

First study of the polymorphic marker MP6D9 in a population of children with cystic fibrosis

https://doi.org/10.71699/revtunbiolclin.v23i1.89

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DOI: https://doi.org/10.71699/revtunbiolclin.v23i1.89

Khaouala Kochbati, Lamia Tilouche, Marwa Mahdouani, Sameh Boughattas, Safia Dahmen, Farah Azouzi, Soumay Ketata, Abdelhalim Trabelsi

Fosfomycin resistance in enterobacteriaceae strains isolated at the CHU Sahloul of Sousse

https://doi.org/10.71699/revtunbiolclin.v29i3.158

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DOI: https://doi.org/10.71699/revtunbiolclin.v29i3.158

H. CHAABOUNI

Genetics in the service of humanity: a century of history

https://doi.org/10.71699/revtunbiolclin.vi15.199

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DOI: https://doi.org/10.71699/revtunbiolclin.vi15.199

Nejia Braham-Jemili, Yosra Ben Youssef, Ines Ghariani, Bechir Achour, Halima Sendi-Sennana, Ali Saad, Abderrahim Khelifi, Monder Kortas

Hematologic characteristics, FAB and WHO classification of 70 cases of myelodysplastic syndroms

https://doi.org/10.71699/revtunbiolclin.v21i1.76

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DOI: https://doi.org/10.71699/revtunbiolclin.v21i1.76

S. HADJ FREDJ, S. OUESLATI, M. BOUDAYA, C. SAHLI, H. SIALA, A. BIBI, T. MESSAOUD

Identification of the cystic fibrosis mutation R334W in a libyan family

https://doi.org/10.71699/revtunbiolclin.v20i2.186

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DOI: https://doi.org/10.71699/revtunbiolclin.v20i2.186

Afif Ba, Manel Ayoub, Sana Aboulkacem, Zied Aouni, Chakib Mazigh

Interleukin 6 polymorphism and acute coronary syndrome

https://doi.org/10.71699/revtunbiolclin.v28i3.138

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DOI: https://doi.org/10.71699/revtunbiolclin.v28i3.138

Nouha Bouayed Abdelmoula

Messenger RNA, the new therapeutic star of the 21st century

https://doi.org/10.71699/revtunbiolclin.v30i3.181

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DOI: https://doi.org/10.71699/revtunbiolclin.v30i3.181

HMIDA SLAMA

MOLECULAR BIOLOGY IN CLINICAL BIOLOGY

https://doi.org/10.71699/revtunbiolclin.vi20.68

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DOI: https://doi.org/10.71699/revtunbiolclin.vi20.68

Rym Kefi-Ben Atig, Houyam Ouragini, Sonia Abdelhak

1-3

Molecular Investigation of Genetic Diseases in Tunisia.

https://doi.org/10.71699/revtunbiolclin.vi21.48

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DOI: https://doi.org/10.71699/revtunbiolclin.vi21.48

I. FODHA, M. RIANI, S. KACEM, M. BEN HAJ FREDJ, S. KETATA, A. LETAIEF, S. AJMI, N. BOUJAAFAR, A. TRABELSI

25-32

Optimization of molecular methodology for the detection of Hepatitis B Virus precore/BCP mutations and analysis of the risk to develop cirrhosis in the center of Tunisia

https://doi.org/10.71699/revtunbiolclin.vi24.64

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DOI: https://doi.org/10.71699/revtunbiolclin.vi24.64

Taieb Messaoud, Ghaya Merdassi, Chakib Mazigh, Sélima Ferchich, Olfa Bahri, Elyes Slim Ghedira, Nejib Barouni, Wadie Khrouf, Haitham Jguirim, Hamdi Dhaouadi, Anis Ben Amor , Noomen Battita

Recommendations of the Standardization Commission maternal serum markers

https://doi.org/10.71699/revtunbiolclin.v28i1.129

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DOI: https://doi.org/10.71699/revtunbiolclin.v28i1.129

H. CHAHED, S. FERCHCHI, Y. CHAABOUNI, N. SAAFI, H. BEN LIMEM, M. SAKOUHI, M. BERNARD, H. KHAIRI, S. LARADI, A. MILED

32-37

Sequential screening of trisomy 21 : experience of the center of Tunisia

https://doi.org/10.71699/revtunbiolclin.vi24.65

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DOI: https://doi.org/10.71699/revtunbiolclin.vi24.65

Roua Talbi , Nabila Ben Rejeb , Slim Kacem , Mohamed Ben Rejeb , Asma Ferjeni , Asma Omezzine , Essia Boughzela , Ali Bouslama

Severity of coronary artery disease is significantly lowered among carriers of The allele 2 of the common apoE polymorphism