Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Zineb Kindil"'
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:
Sanaa Nassereddine, Zouhair Elkarhat, Chadli Elbakay, Latifa Zarouf, Zineb Kindil, Abdelhamid Barakat, Jamila Aboulfaraj, Hassan Rouba, Boubker Nasser, Lunda Razoki
Publikováno v:
Journal of Assisted Reproduction and Genetics. 36:499-507
PURPOSE: The aim of this study is to evaluate the frequency and nature of chromosomal abnormalities in Moroccan couples with recurrent spontaneous miscarriage (RSM). In addition, the data were compared with those reported elsewhere in order to give a
Autor:
Sellama Nadifi, Zineb Kindil, Soumia Chihab, Hicham Charoute, Abdelhamid Barakat, Mohamed Amine Senhaji, Amina Bakhchane
Publikováno v:
BMC Research Notes
BMC Research Notes, Vol 10, Iss 1, Pp 1-6 (2017)
BMC Research Notes, Vol 10, Iss 1, Pp 1-6 (2017)
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, the XP gr
Autor:
Rachida Roky, Amina Bakhchane, K. Khadir, Sellama Nadifi, K. Baline, K. Benchikhi, Abdelhamid Barakat, Hicham Charoute, Zineb Kindil
Publikováno v:
Current research in translational medicine. 64(2)
H syndrome is an autosomal recessive syndrome, which affects the skin and some vital organs, it is caused by mutations in the SLC29A3 gene, encoding the human equilibrative nucleoside transporter hENT3. This report describes a patient with typical fe