Dimassi Sarra - CRNL, CNRS UMR 5292, INSERM U1028, Lyon, France; Department of Genetics, Lyon University Hospital, Lyon, France; Claude Bernard Lyon I University, Lyon, France.

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论文共 24 篇作者统计合作学者相似作者

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Steroid sulfatase deficiency in Tunisian patients: awareness of STS pseudogene technical trap

Hamza Chouk,Sarra Saad,Rima Gammoudi,Lobna Boussofara,Sarra Dimassi,Ali Saad,Mohamed Denguezli,Dorra H'mida

EUROPEAN JOURNAL OF HUMAN GENETICS (2023): 129-129

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Additional evidence for the role of chromosomal imbalances and SOX8, ZNRF3 and HHAT gene variants in early human testis development

Khouloud Rjiba,Soumaya Mougou-Zerelli, Imen hadj Hamida,Ghada Saad,Bochra Khadija,Afef Jelloul,Wafa Slimani,Yosra Hasni,Sarra Dimassi,Hela Ben khelifa,Amira Sallem,Molka Kammoun,

Reprod Biol Endocrinol（2023）

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58P Molecular investigation using microarray-based comparative genomic hybridization in patients with myelodysplastic syndrome and normal karyotype

M.A.N. Ammar,A. Bennour, I. Ouahchi, L. Yahia,S. Dimassi, S. Mougou, A. Saad, D. H'Mida, H. Sennana

ESMO Openno. 1 (2023): 101868-101868

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Alfi syndrome in a patient with ring chromosome 9

Amira Benzarti, Abdallah Ghourabi,Mohamed Ali Ksentini, Noomen Batita,Ali Saad,Sarra Dimassi

EUROPEAN JOURNAL OF HUMAN GENETICS (2023): 278-278

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Clinical and molecular characterization of 1q43q44 deletion and corpus callosum malformations: 2 new cases and literature review

Bochra Khadija,Khouloud Rjiba,Sarra Dimassi, Wafa Dahleb,Molka Kammoun, Hanen Hannechi,Najoua Miladi,Neziha Gouider-khouja,Ali Saad,Soumaya Mougou-Zerelli

Molecular Cytogeneticsno. 1 (2022): 1-12

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X-linked recessive ichthyosis in 8 Tunisian patients: awareness of misdiagnosis due to the technical trap of the STS pseudogene

Hamza CHOUK,Sarra SAAD,Sarra DIMASSI,Nadia GHARIANI FETOUI,Ayda BENNOUR,Rima GAMMOUDI,Haifa ELMABROUK,Ali SAAD,Mohamed DENGUEZLI,Dorra H’MIDA

Research Square (Research Square) (2022)

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X-linked recessive ichthyosis in 8 Tunisian patients: awareness of misdiagnosis due to the technical trap of the STS pseudogene

Hamza Chouk,Sarra Saad,Sarra Dimassi,Nadia Ghariani Fetoui,Ayda Bennour,Rima Gammoudi,Haifa Elmabrouk,Ali Saad,Mohamed Denguezli,Dorra H’mida

BMC Med Genomics（2022）

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Neuronal migration genes and a familial translocation t (3;17): candidate genes implicated in the phenotype

Meriam Hadj Amor,Sarra Dimassi,Amel Taj,Wafa Slimani,Hanene Hannachi, Adnene Mlika, Khaled Ben Helel,Ali Saad,Soumaya Mougou-Zerelli

BMC medical genetics（2020）

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A rare case of partial monosomy 7p22.3p22.1 and partial trisomy 8q24.23q24.3

Rahma Touhami,Soumaya Mougou Zerelli, Ilhem Ben Youssef,Sarra Dimassi,Ali Saad,Damien Sanlaville,Amel Haj Khelil

MOLECULAR CYTOGENETICS（2019）

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fishing with the ring

S. Dimassi, Y. Halleb, N. Kahloul, W. Gafsi, A. Jalloul,H. Hadj Abdallah, L. Boughammoura,S. Mougou-Zerelli,A. Saad

EUROPEAN JOURNAL OF HUMAN GENETICS（2019）

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