Lista de obras -

A mutation in PNPT1, encoding mitochondrial-RNA-import protein PNPase, causes hereditary hearing loss

artículo científico publicado en 2012

A novel mutation in the Espin gene causes autosomal recessive nonsyndromic hearing loss but no apparent vestibular dysfunction in a Moroccan family.

artículo científico publicado en 2008

AZF microdeletions and partial deletions of AZFc region on the Y chromosome in Moroccan men.

artículo científico publicado en 2007

Absence of GJB3 and GJB6 mutations in Moroccan familial and sporadic patients with autosomal recessive non-syndromic deafness

artículo científico publicado en 2008

Allele frequencies and population data for 17 Y-STR loci (The AmpFlSTR® Y-filer™) in Casablanca resident population

artículo científico publicado en 2010

Analysis of CLDN14 gene in deaf Moroccan patients with non-syndromic hearing loss

artículo científico publicado en 2013

Analysis of MYO7A in a Moroccan family with Usher syndrome type 1B: novel loss-of-function mutation and non-pathogenicity of p.Y1719C.

artículo científico publicado en 2007

Association analysis of IGF2BP2, KCNJ11, and CDKAL1 polymorphisms with type 2 diabetes mellitus in a Moroccan population: a case-control study and meta-analysis.

artículo científico publicado en 2014

Cancer incidence in eastern Morocco: cancer patterns and incidence trends, 2005-2012

artículo científico

Carrier frequencies of mutations/polymorphisms in the connexin 26 gene (GJB2) in the Moroccan population

artículo científico publicado en 2008

Distribution and features of hematological malignancies in Eastern Morocco: a retrospective multicenter study over 5 years

artículo científico publicado en 2016

GJB2 (connexin 26) gene mutations in Moroccan patients with autosomal recessive non-syndromic hearing loss and carrier frequency of the common GJB2-35delG mutation.

artículo científico publicado en 2007

Genetic and molecular analysis of the CLDN14 gene in Moroccan family with non-syndromic hearing loss.

artículo científico publicado en 2013

Maternal effect and familial aggregation in a type 2 diabetic Moroccan population.

artículo científico publicado en 2011

Molecular analysis of the TMPRSS3 gene in Moroccan families with non-syndromic hearing loss.

artículo científico publicado en 2012

Morocco's First Biobank: Establishment, Ethical Issues, Biomedical Research Opportunities, and Challenges

artículo científico publicado en 2020

Mutation rate at 17 Y-STR loci in "Father/Son" pairs from moroccan population

artículo científico publicado en 2013

Mutations in TPRN cause a progressive form of autosomal-recessive nonsyndromic hearing loss

artículo científico publicado en 2010

No association between T222P/LGR8 mutation and cryptorchidism in the Moroccan population

artículo científico publicado en 2008

Novel compound heterozygous MYO7A mutations in Moroccan families with autosomal recessive non-syndromic hearing loss

artículo científico publicado en 2017

Patients' Knowledge and Attitude Toward Biobanks in Eastern Morocco

artículo científico publicado en 2020

Prevalence of the mitochondrial A 1555G mutation in Moroccan patients with non-syndromic hearing loss

artículo científico publicado en 2010

Recessive TBC1D24 Mutations Are Frequent in Moroccan Non-Syndromic Hearing Loss Pedigrees

artículo científico publicado en 2015

The analysis of three markers flanking GJB2 gene suggests a single origin of the most common 35delG mutation in the Moroccan population

artículo científico publicado en 2008

The c.242G>A mutation in LRTOMT gene is responsible for a high prevalence of deafness in the Moroccan population

artículo científico publicado en 2012

[Lung cancer in Eastern Morocco: where do we stand?]

artículo científico publicado en 2019

Lista de obras de

A mutation in PNPT1, encoding mitochondrial-RNA-import protein PNPase, causes hereditary hearing loss

A novel mutation in the Espin gene causes autosomal recessive nonsyndromic hearing loss but no apparent vestibular dysfunction in a Moroccan family.

AZF microdeletions and partial deletions of AZFc region on the Y chromosome in Moroccan men.

Absence of GJB3 and GJB6 mutations in Moroccan familial and sporadic patients with autosomal recessive non-syndromic deafness

Allele frequencies and population data for 17 Y-STR loci (The AmpFlSTR® Y-filer™) in Casablanca resident population

Analysis of CLDN14 gene in deaf Moroccan patients with non-syndromic hearing loss

Analysis of MYO7A in a Moroccan family with Usher syndrome type 1B: novel loss-of-function mutation and non-pathogenicity of p.Y1719C.

Association analysis of IGF2BP2, KCNJ11, and CDKAL1 polymorphisms with type 2 diabetes mellitus in a Moroccan population: a case-control study and meta-analysis.

Cancer incidence in eastern Morocco: cancer patterns and incidence trends, 2005-2012

Carrier frequencies of mutations/polymorphisms in the connexin 26 gene (GJB2) in the Moroccan population

Distribution and features of hematological malignancies in Eastern Morocco: a retrospective multicenter study over 5 years

GJB2 (connexin 26) gene mutations in Moroccan patients with autosomal recessive non-syndromic hearing loss and carrier frequency of the common GJB2-35delG mutation.

Genetic and molecular analysis of the CLDN14 gene in Moroccan family with non-syndromic hearing loss.

Maternal effect and familial aggregation in a type 2 diabetic Moroccan population.

Molecular analysis of the TMPRSS3 gene in Moroccan families with non-syndromic hearing loss.

Morocco's First Biobank: Establishment, Ethical Issues, Biomedical Research Opportunities, and Challenges

Mutation rate at 17 Y-STR loci in "Father/Son" pairs from moroccan population

Mutations in TPRN cause a progressive form of autosomal-recessive nonsyndromic hearing loss

No association between T222P/LGR8 mutation and cryptorchidism in the Moroccan population

Novel compound heterozygous MYO7A mutations in Moroccan families with autosomal recessive non-syndromic hearing loss

Patients' Knowledge and Attitude Toward Biobanks in Eastern Morocco

Prevalence of the mitochondrial A 1555G mutation in Moroccan patients with non-syndromic hearing loss

Recessive TBC1D24 Mutations Are Frequent in Moroccan Non-Syndromic Hearing Loss Pedigrees

The analysis of three markers flanking GJB2 gene suggests a single origin of the most common 35delG mutation in the Moroccan population

The c.242G>A mutation in LRTOMT gene is responsible for a high prevalence of deafness in the Moroccan population

[Lung cancer in Eastern Morocco: where do we stand?]