Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Faiza Chbel"'
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 25, Iss 1, Pp 1-6 (2024)
Abstract Background WAGR syndrome is a rare genetic disorder characterized by a de novo deletion of 11p13 and is usually clinically associated with Wilms’ tumor, aniridia, genitourinary anomalies, and mental retardation (W-A-G-R). Although the geno
Externí odkaz:
https://doaj.org/article/3c6bc4dc111d4b6b9b947a50b1ba0088
Autor:
Hasna Hamdaoui, Badreddine Nouadi, Oumaima Benlarroubia, Faiza Chbel, Chaimaa Saadoune, Faïza Bennis, Afaf Lamzouri, Fatima Chegdani
Publikováno v:
Leukemia Research Reports, Vol 20, Iss , Pp 100392- (2023)
Background: The nonrandom recurrence of chromosomal abnormalities in multiple myeloma (MM) raises the possibility that they play a role in the pathophysiology and development of the disease. Fluorescence in situ hybridization (FISH) can identify a hi
Externí odkaz:
https://doaj.org/article/20d0807d94b841d7a5e76227cac6c4b7
Autor:
Faiza Chbel, Hicham Charroute, Redouane Boulouiz, Hasna Hamdaoui, Houssein Mossafa, Houda Benrahma, Karim Ouldim
Publikováno v:
Clinical Case Reports, Vol 10, Iss 3, Pp n/a-n/a (2022)
Abstract Myoclonus–dystonia (M‐D) is a pleiotropic neuropsychiatric disorder with autosomal dominant mode of inheritance with variable severity and incomplete penetrance. Pathogenic variants in ξ‐sarcoglycan gene SGCE are the most frequently k
Externí odkaz:
https://doaj.org/article/f486de72d0eb43009a9c5bd19443f981
Autor:
Hamdaoui Hasna, Abdelhafid Natiq, Oumaima Benlarroubia, Faiza CHBEL, Rajaa Chahboun, jihane Toughza, Afaf Lamzouri
Cup Like acute myeloid leukemia is the rarest form of children leukemia. We present a case of Cup Like Acute Myeloid Leukemia (AML) with t(4;12) (q12;p13) associated with two other clones t(1;16)(q12;q24) and t(12;13)(p13;q13). Cytogenetic and iFISH
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e2b79f0629d5e33205b8f23b956668ca
https://doi.org/10.22541/au.166661107.77254644/v1
https://doi.org/10.22541/au.166661107.77254644/v1
Autor:
Karen Rouault, Claude Férec, Orla Hardiman, Miriam Baeta, Faiza Chbel, Ana Díaz-de Usera, Carolina Núñez, Fátima Pinheiro, Marian M. de Pancorbo, Endika Prieto-Fernández, Sellama Nadifi
Publikováno v:
Forensic science international. Genetics. 27
The forensic use of X-STRs requires the creation of allele and haplotype frequency databases in the populations where they are going to be used. Recently, an updated Spanish allele and haplotype frequency database for the new 17 X-STR panel has been
Autor:
Luis Bujanda, Faiza Chbel, Dora Sánchez, David Celorrio, Marian M. de Pancorbo, Begoña Martínez-Jarreta
Publikováno v:
Alcoholism: Clinical and Experimental Research. 35:879-884
Background: Genes ADH1B and ADH1C have certain functional SNPs that are related toalcoholism. The frequencies of these polymorphisms vary between populations, so studying themin populations made up of groups with different phylogeographic origins req
Publikováno v:
Forensic Science International: Genetics. 7:e90-e92
Autor:
Sellama Nadifi, M. M. de Pancorbo, Maite Alvarez-Alvarez, Houssine Azeddoug, Faiza Chbel, C Martı́nez-Bouzas, M.-J. Rodriguez-Tojo
Publikováno v:
Russian Journal of Genetics. 39:1184-1190
Alu elements are the largest family of short tandem interspersed elements (SINEs) in human who have arisen to a copy number with an excess of 500 000 copies per haploid human genome and mobilize through an RNAse polymerase III derived transcript in a
Publikováno v:
Molecular Ecology Notes. 2:484-487
Here we present a new set of 22 microsatellite loci isolated from Chlamydotis undulata undulata, an endangered Houbara bustard found across North Africa. The number of alleles per locus ranged from one to nine, and heterozygosities ranged from 0.167
Autor:
Brahim El Houate, Faiza Chbel, Adil Laouina, Jalal Talbi, Sellama Nadifi, Hakima Yahia, Redouane Boulouiz, Marzouk El Arji
Publikováno v:
Legal medicine (Tokyo, Japan). 15(5)
Precise knowledge of mutation rate at Y-STRs loci is essential for a correct evaluation of typing results in forensic casework and specially kinship genetic studies. In this study, we have examined 252 confirmed and unrelated father/son sample pairs