Guipponi, M. Et Al. 2022. A homozygous duplication of the FGG exon 8-intron 8 junction causes congenital afibrinogenemia. Lessons learned from the Turkish study family of a large consanguineous. Haematologica , vol.107, no.5 , 1064-1071.

Guipponi, M., Masclaux, F., Sloan-Béna, F., Sanza, C. D., Özbek, N., Peyvandi, F., ... Menegatti, M.(2022). A homozygous duplication of the FGG exon 8-intron 8 junction causes congenital afibrinogenemia. Lessons learned from the Turkish study family of a large consanguineous. Haematologica , vol.107, no.5, 1064-1071.

Guipponi, Michel Et Al. "A homozygous duplication of the FGG exon 8-intron 8 junction causes congenital afibrinogenemia. Lessons learned from the Turkish study family of a large consanguineous," Haematologica , vol.107, no.5, 1064-1071, 2022

Guipponi, Michel Et Al. "A homozygous duplication of the FGG exon 8-intron 8 junction causes congenital afibrinogenemia. Lessons learned from the Turkish study family of a large consanguineous." Haematologica , vol.107, no.5, pp.1064-1071, 2022

Guipponi, M. Et Al. (2022) . "A homozygous duplication of the FGG exon 8-intron 8 junction causes congenital afibrinogenemia. Lessons learned from the Turkish study family of a large consanguineous." Haematologica , vol.107, no.5, pp.1064-1071.

@article{article, author={Michel Guipponi Et Al. }, title={A homozygous duplication of the FGG exon 8-intron 8 junction causes congenital afibrinogenemia. Lessons learned from the Turkish study family of a large consanguineous}, journal={Haematologica}, year=2022, pages={1064-1071} }