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Author/Creator Hizem, Syrine

2. Beckwith–Wiedemann syndrome: Clinical, histopathological and molecular study of two Tunisian patients and review of literature. Issue 10 (12th September 2021)

Authors:
Sassi, Hela; Elaribi, Yasmina; Jilani, Houweyda; Rejeb, Imen; Hizem, Syrine; Sebai, Molka; Kasdallah, Nadia; Bouthour, Habib; Hannachi, Samia; Beygo, Jasmin; Saad, Ali; Buiting, Karin; H'mida Ben‐Brahim, Dorra; BenJemaa, Lamia
Journal:
Molecular genetics & genomic medicine
Issue:
Volume 9:Issue 10(2021)
Page Start:
n/a
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

4. In vitro functional characterization of the novel DHH mutations p.(Asn337Lysfs*24) and p.(Glu212Lys) associated with gonadal dysgenesis. Issue 12 (22nd October 2018)

Authors:
Tajouri, Asma; Kharrat, Maher; Hizem, Syrine; Zaghdoudi, Hajer; M'rad, Ridha; Simic‐Schleicher, Gunter; Kaiser, Frank J.; Hiort, Olaf; Werner, Ralf
Journal:
Human mutation
Issue:
Volume 39:Issue 12(2018)
Page Start:
2097
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗