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Books & Literature
Halima Nahili | XanEdu Customization Platform
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Author: Halima Nahili. Results. Maternal Effect and Familial Aggregation in a Type 2 Diabetic Moroccan Population Springer Science+Business Media ...
- مقالات نوشته شده توسط Halima Nahili سایپرز، باشگاه دانش
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A novel mutation in the TMC1 gene causes non-syndromic hearing loss in a Moroccan family. سال انتشار: Available online 28 July ژورنال: Gene نویسنده ...
Related Documents
Prediction of the Impact of Deleterious Nonsynonymous ...search.ebscohost.com › login
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and Halima Nahili Laboratory of Genomics and Human Genetics, Institut Pasteur du Maroc, Casablanca, Morocco. 2Laboratory of ...
Genetic and molecular analysis of the CLDN14 gene in Moroccan family...
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Authors: Majida Charif, Redouane Boulouiz, Amina Bakhechane, Houda Benrahma, Halima Nahili, Abdelmajid Eloualid, Hassan Rouba, Mostafa Kandil, Omar ...
Scientific Publications
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Amina Bakhchane, Hicham Charoute, Halima Nahili, Rachida Roky, Hassan Rouba ... The gene modules sensitive to various cardiac disease-related perturbations ...
A novel mutation in the TMC1 gene causes non PubMedpubmed.ncbi.nlm.nih.gov › ...
pubmed.ncbi.nlm.nih.gov
Authors. Amina Bakhchane , Hicham Charoute , Halima Nahili , Rachida Roky , Hassan Rouba , Majida Charif , Guy Lenaers , Abdelhamid Barakat ...
Recessive TBC1D24 Mutations Are Frequent in Moroccan NCBI
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Boulouiz, 1Halima Nahili, 1 Rachida Roky, 2 Guy Lenaers,# 3 , 4 and ...
Halima Nahili – ScienceOpen
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Mutations in the connexin 26 gene (GJB2), which encodes a gap-junction protein expressed in the inner ear, have been shown to be responsible for a major part ...
Publications
Prediction of the Impact of Deleterious Hindawiwww.hindawi.com › journals › bmri
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Chaimaa Ait El Cadi, Al Mehdi Krami, Hicham Charoute, Zouhair Elkarhat, Najat Sifeddine, Hamid Lakhiari, Hassan Rouba, Abdelhamid Barakat, Halima Nahili, ...
Maternal Effect and Familial Aggregation in a Type 2 Diabetic...
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The aim of this study is to evaluate the degree of familial aggregation of type 2 diabetes mellitus in Morocco and to investigate transmission patterns of
Halima Nahili's Research | CureHunter
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Halima Nahili Selected Research. Halima Nahili Research Topics. Disease. 4, Hearing Loss (Hearing Impairment) , Disease Susceptibility ...
Miscellaneous
halima nahili | LinkedIn
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View halima nahili's professional profile on LinkedIn. LinkedIn is the world's largest business network, helping professionals like halima nahili discover inside ...
Halima Nahili
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Halima Nahili. Details · Publications ... Halima Nahili, Mohamed Ridal, Redouane Boulouiz, Omar Abidi, more · International Journal of Pediatric ...
Infertility: Nahili, Halima - Expertscape.com
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Halima Nahili has special expertise in Infertility
(PDF) Recessive TBC1D24 Mutations Are Frequent in Moroccan...
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Recessive TBC1D24 Mutations Are Frequent in Moroccan Non-Syndromic Hearing Loss Pedigrees
(PDF) A novel mutation in the TMC1 gene causes non-syndromic hearing...
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A novel mutation in the TMC1 gene causes non-syndromic hearing loss in a Moroccan family
Asian Journal of Andrology
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Laila Imken, Brahim El Houate, Abdelaziz Chafik, Halima Nahili, Redouane Boulouiz, Omar Abidi, Elbakkay Chadli, Noureddine Louanjli, Abdelouhab Elfath, ...
(PDF) The analysis of three markers flanking GJB2 gene suggests a...
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The analysis of three markers flanking GJB2 gene suggests a single origin of the most common 35delG mutation in the Moroccan population
A novel mutation in SLITRK6 causes deafness and myopia in ...read.qxmd.com › read › a-novel-mutation-in-slitrk6-ca...
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Sara Salime, Zied Riahi, Soukaina Elrharchi, Lamiae Elkhattabi, Hicham Charoute, Halima Nahili, Hassan Rouba, Mostafa Kabine, Crystel Bonnet, Christine ...
Gale Academic OneFile - Document - Carrier frequencies of...
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Carrier frequencies of mutations/polymorphisms in the connexin 26 gene (GJB2) in the Moroccan population. Omar Abidi, Redouane Boulouiz, Halima Nahili, ...
A novel mutation in the TMC1 gene causes non-syndromic hearing loss...
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Amina Bakhchane, Hicham Charoute, Halima Nahili, Rachida Roky, Hassan Rouba, et al.. A novel mutation in the TMC1 gene causes non-syndromic hearing ...
Recessive TBC1D24 Mutations Are Frequent in Moroccan Non-Syndromic...
hal.archives-ouvertes.fr
Halima Nahili, et al.. Recessive TBC1D24 Mutations Are Frequent in Moroccan ...
AZF microdeletions and partial deletions of AZFc region on the ...cyberleninka.org › article
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... scientific paper in Biological sciences , author of scholarly article — Laila Imken, Brahim El Houate, Abdelaziz Chafik, Halima Nahili, Redouane Boulouiz, et al.
Carrier frequencies of mutations/polymorphisms in the ...go.gale.com › i.do
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Author(s): Omar Abidi, Redouane Boulouiz, Halima Nahili, Khadija Bakhouch, Lahcen Wakrim, Hassan Rouba, . Source: Genetic Testing. Document Type: ...
Schematic representation of the mutations responsible for non ...
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Redouane Boulouiz Halima Nahili Rachida Roky Guy Lenaers Abdelhamid ...
First characterization of LHON pedigrees in North X-MOLwww.x-mol.com › paper
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... Amalou,David Goudenège,Valérie Desquiret-Dumas,Céline Bris,Najat Sifeddine,Halima Nahili,Meriem Elqabli,Kenza Dafir,Mostafa Kandil ...
CrossRef TDM - Journal of Audiology & Otologywww.ejao.org › journal › crossRefTDM
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Omar Abidi, Redouane Boulouiz, Halima Nahili, Mohammed Ridal, Mohamed Noureddine Alami, Abdelaziz Tlili, Hassan Rouba, Saber ...
Absence of GJB3 and GJB6 mutations in Moroccan familial and ...
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Halima Nahili · Mohamed Ridal · Redouane Boulouiz · Omar Abidi · Laila Imken · Hassan Rouba · Mohammed Noureddine Alami · Abdelaziz ...
SpringerCitations - Details Page
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Article. Prevalence of the mitochondrial A 1555G mutation in Moroccan patients with non-syndromic hearing loss. Halima Nahili, Majida Charif, Redouane Boulouiz, Safaa ...
Back - Medknow Publications: Publisher of peer reviewed scholarly ...
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Majida Charif, Redouane Boulouiz, Amina Bakhechane, Houda Benrahma, Halima Nahili, Abdelmajid Eloualid, Hassan Rouba, Mostafa Kandil, Omar Abidi, ...
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