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Transfusion Clinique Et Biologique : Journal De La Societe Francaise De Transfusion Sanguine|January 26, 2023
Transfusion management of Africans with RHD variants in ChinaQinan Yin, Mouna Ouchari
Saudi Journal of Biological Sciences|August 16, 2018
Autosomal single-gene disorders involved in human infertilityInes Jedidi, Mouna Ouchari, Qinan Yin
European Journal of Medical Genetics|August 13, 2019
Sex chromosomes-linked single-gene disorders involved in human infertilityInes Jedidi, Mouna Ouchari, Qinan Yin
Cell Transplantation|August 25, 2020
In Vitro Generation of Red Blood Cells from Stem Cell and Targeted TherapyPing Zhou, Mouna Ouchari, Yun Xue, et al.
Transfusion Clinique Et Biologique : Journal De La Societe Francaise De Transfusion Sanguine|May 15, 2021
Transfusion management of a Chinese pregnant woman with RHD*DEL1 alleleChunyan Liu, Yun Xue, Mouna Ouchari, et al.
Transfusion|December 2, 2017
Transfusion strategy for weak D Type 4.0 based on RHD alleles and RH haplotypes in TunisiaMouna Ouchari, Kshitij Srivastava, Houda Romdhane, et al.
Asian Journal of Transfusion Science|September 10, 2013
RHD alleles in the Tunisian populationMouna Ouchari, Saloua Jemni-Yaacoub, Taher Chakroun, et al.
Transfusion and Apheresis Science : Official Journal of the World Apheresis Association : Official Journal of the European Society for Haemapheresis|December 3, 2014
RHD genotyping and its implication in transfusion practiceAwatef Sassi, Mouna Ouchari, Batoul Houissa, et al.
Blood Transfusion = Trasfusione Del Sangue|November 5, 2014
Weak D in the Tunisian populationMouna Ouchari, Houda Romdhane, Taher Chakroun, et al.
Transfusion|November 22, 2014
Short duplication within the RHCE gene associated with an in cis deleted RHD causing a Rhnull amorph phenotype in an immunized pregnant woman with anti-Rh29Monique Silvy, Sophie Beley, Thierry Peyrard, et al.
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