Canlyniadau Chwilio - Sonia Abdelhak
- Dangos 1 - 5 canlyniadau o 5
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1
Mitochondrial DNA structure of an isolated Tunisian Berber population and its relationship with Mediterranean populations gan Nizar Ben Halim, Sana Hsouna, Khaled Lasram, Mariem Chargui, Laaroussi Khemira, Rachid Saidane, Sonia Abdelhak, Rym Kefi
Cyhoeddwyd 2018Rhif Galw: Llwytho...Connect to this object online.
Wedi'i leoli: Llwytho...
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2
Using KASP technique to screen LRRK2 G2019S mutation in a large Tunisian cohort gan Zied Landoulsi, Sawssan Benromdhan, Mouna Ben Djebara, Mariem Damak, Hamza Dallali, Rym Kefi, Sonia Abdelhak, Amina Gargouri-Berrechid, Chokri Mhiri, Riadh Gouider
Cyhoeddwyd 2017Rhif Galw: Llwytho...Connect to this object online.
Wedi'i leoli: Llwytho...
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3
Alopecia patterns and trichoscopic findings in patients with autosomal recessive congenital ichthyosis gan Anissa Zaouak, MD, Wafa Jouini, MD, Ghaith Abdessalem, PhD, Sonia Abdelhak, PhD, Houda Hammami, MD, Cherine Charfeddine, PhD, Samy Fenniche, MD
Cyhoeddwyd 2024Rhif Galw: Llwytho...Connect to this object online.
Wedi'i leoli: Llwytho...
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4
Clinical and Genetic Heterogeneity in Six Tunisian Families With Horizontal Gaze Palsy With Progressive Scoliosis: A Retrospective Study of 13 Cases gan Sami Bouchoucha, Sami Bouchoucha, Asma Chikhaoui, Dorra Najjar, Hamza Dallali, Maleke Khammessi, Sonia Abdelhak, Nabil Nessibe, Mohammad Shboul, Susanne G. Kircher, Ali Al Kaissi, Ali Al Kaissi, Houda Yacoub-Youssef
Cyhoeddwyd 2020Rhif Galw: Llwytho...Connect to this object online.
Wedi'i leoli: Llwytho...
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5
Clinical profile of comorbidity of rare diseases in a Tunisian patient: a case report associating incontinentia pigmenti and Noonan syndrome gan Nehla Ghedira, Arnaud Lagarde, Karim Ben Ameur, Sahar Elouej, Rania Sakka, Emna Kerkeni, Fatma-Zohra Chioukh, Sylviane Olschwang, Jean-Pierre Desvignes, Sonia Abdelhak, Valerie Delague, Nicolas Lévy, Kamel Monastiri, Annachiara De Sandre-Giovannoli
Cyhoeddwyd 2018Rhif Galw: Llwytho...Connect to this object online.
Wedi'i leoli: Llwytho...
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