M. Ben Khelifa

发表

A recurrent deletion of DPY19L2 causes infertility in man by blocking sperm head elongation and acrosome formation.

P. Jouk, S. Viville, F. Abada, 2011, American journal of human genetics.

Mutations in DNAH1, which encodes an inner arm heavy chain dynein, lead to male infertility from multiple morphological abnormalities of the sperm flagella.

N. Thierry-Mieg, D. Grunwald, P. Jouk, 2014, American journal of human genetics.

DPY19L2 deletion as a major cause of globozoospermia.

C. Redin, S. Viville, P. Ray, 2011, American journal of human genetics.

MLPA and sequence analysis of DPY19L2 reveals point mutations causing globozoospermia.

P. Jouk, F. Abada, P. Ray, 2012, Human reproduction.

Identification of a new recurrent aurora kinase C mutation in both European and African men with macrozoospermia.

M. Blum, P. Jouk, S. Viville, 2012, Human reproduction.

A new AURKC mutation causing macrozoospermia: implications for human spermatogenesis and clinical diagnosis.

P. Ray, J. Lunardi, R. Zouari, 2011, Molecular human reproduction.

A MEI1 homozygous missense mutation associated with meiotic arrest in a consanguineous family.

C. Hue, H. Garchon, F. Vialard, 2018, Human reproduction.

Prevalence of Y chromosome microdeletions in infertile Tunisian men.

S. Abdelhak, A. Amouri, M. ben Khelifa, 2014, Annales de biologie clinique.

Genetic causes of macrozoospermia and proposal for an optimized genetic diagnosis strategy based on sperm parameters.

N. Thierry-Mieg, P. Ray, E. Bieth, 2023, Journal of genetics and genomics = Yi chuan xue bao.

A recurrent deletion of DPY19L2 causes infertility in man by blocking sperm head elongation and acrosome formation.

P. Jouk, S. Viville, F. Abada, 2011, American journal of human genetics.