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Autor:
Essadssi, Soukaina, Benhsaien, Ibtihal, Bakhchane, Amina, Charoute, Hicham, Abdelghaffar, Houria, Bousfiha, Ahmed Aziz, Barakat, Abdelhamid
Publikováno v:
Human Heredity, 2020 Jan 01. 84(6), 272-278.
Externí odkaz:
https://www.jstor.org/stable/48635335
Autor:
Bousfiha, Amale, Riahi, Zied, Elkhattabi, Lamiae, Bakhchane, Amina, Charoute, Hicham, Snoussi, Khalid, Bonnet, Crystel, Petit, Christine, Barakat, Abdelhamid
Publikováno v:
Human Heredity, 2019 Jan 01. 84(3), 109-116.
Externí odkaz:
https://www.jstor.org/stable/48635325
Autor:
AitRaise, Imane, Amalou, Ghita, Bakhchane, Amina, Bousfiha, Amale, Abdelghaffar, Houria, Majida, Charif, Bonnet, Crystel, Petit, Christine, Barakat, Abdelhamid
Publikováno v:
Biochemical Genetics; Jun2024, Vol. 62 Issue 3, p1914-1924, 11p
Autor:
Salime, Sara, Charif, Majida, Bousfiha, Amale, Elrharchi, Soukaina, Bakhchane, Amina, Charoute, Hicham, Kabine, Mostafa, Snoussi, Khalid, Lenaers, Guy, Barakat, Abdelhamid
Publikováno v:
In International Journal of Pediatric Otorhinolaryngology October 2017 101:25-29
Autor:
Zineb Kindil, Mohamed Amine Senhaji, Amina Bakhchane, Hicham Charoute, Soumia Chihab, Sellama Nadifi, Abdelhamid Barakat
Publikováno v:
BMC Research Notes, Vol 10, Iss 1, Pp 1-6 (2017)
Abstract Objective Xeroderma pigmentosum (XP) is a genetically and clinically heterogeneous disease, associated with an inherited defect in one of eight different genes (XPA to XPG and XPV). In addition to the early onset of the skin manifestations,
Externí odkaz:
https://doaj.org/article/0add5980e7164b9a8a081a7cfa58c7cb
Autor:
Bakhchane, Amina, Bousfiha, Amale, Charoute, Hicham, Salime, Sara, Detsouli, Mustapha, Snoussi, Khalid, Nadifi, Sellama, Kabine, Mostafa, Rouba, Hassan, Dehbi, Hind, Roky, Rachida, Charif, Majida, Barakat, Abdelhamid
Publikováno v:
In European Journal of Medical Genetics June 2016 59(6-7):325-329
Autor:
Bousfiha, A., Bakhchane, A., Elrharchi, S., Dehbi, H., Kabine, M., Nadifi, S., Charoute, H., Barakat, A.
Publikováno v:
In Current Research in Translational Medicine April-June 2016 64(2):61-64
Autor:
Amina Bakhchane, Majida Charif, Amale Bousfiha, Redouane Boulouiz, Halima Nahili, Hassan Rouba, Hicham Charoute, Guy Lenaers, Abdelhamid Barakat
Publikováno v:
PLoS ONE, Vol 12, Iss 5, p e0176516 (2017)
The MYO7A gene encodes a protein belonging to the unconventional myosin super family. Mutations within MYO7A can lead to either non syndromic hearing loss or to the Usher syndrome type 1B (USH1B). Here, we report the results of genetic analyses perfo
Externí odkaz:
https://doaj.org/article/82f455cff15345659651dafe589d5c76
Autor:
Benhsaien, Ibtihal, Essadssi, Soukaina, Elkhattabi, Lamiae, Bakhchane, Amina, Abdelghaffar, Houria, Bousfiha, Ahmed Aziz, Badou, Abdallah, Barakat, Abdelhamid
Publikováno v:
In Immunobiology May 2021 226(3)