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

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 of spermatogenic failure with the b2/b3 partial AZFc deletion

artículo científico publicado en 2012

Association of the C677T polymorphism in the human methylenetetrahydrofolate reductase (MTHFR) gene with the genetic predisposition for type 2 diabetes mellitus in a Moroccan population

artículo científico publicado en 2011

Association of the MTHFR A1298C variant with unexplained severe male infertility

artículo científico publicado en 2012

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

artículo científico publicado en 2008

Clinicopathological features and molecular analysis of primary glioblastomas in Moroccan patients

artículo científico publicado en 2012

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

Methylenetetrahydrofolate Reductase Gene Polymorphisms (C677T and A1298C) and Hemorrhagic Stroke in Moroccan Patients.

artículo científico publicado en 2018

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

artículo científico publicado en 2012

Mutational analysis of the RB1 gene in Moroccan patients with retinoblastoma

artículo científico publicado en 2011

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

artículo científico publicado en 2010

TNF A -308G>A polymorphism in Moroccan patients with type 2 diabetes mellitus: a case-control study and meta-analysis

artículo científico publicado en 2014

The Moroccan Genetic Disease Database (MGDD): a database for DNA variations related to inherited disorders and disease susceptibility

artículo científico publicado en 2013

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

The prevalence of resistance-associated mutations to protease and reverse transcriptase inhibitors in treatment-naïve (HIV1)-infected individuals in Casablanca, Morocco.

artículo científico publicado en 2009

c.1643_1644delTG XPC mutation is more frequent in Moroccan patients with xeroderma pigmentosum.

artículo científico publicado en 2012

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

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 of spermatogenic failure with the b2/b3 partial AZFc deletion

Association of the C677T polymorphism in the human methylenetetrahydrofolate reductase (MTHFR) gene with the genetic predisposition for type 2 diabetes mellitus in a Moroccan population

Association of the MTHFR A1298C variant with unexplained severe male infertility

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

Clinicopathological features and molecular analysis of primary glioblastomas in Moroccan patients

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.

Methylenetetrahydrofolate Reductase Gene Polymorphisms (C677T and A1298C) and Hemorrhagic Stroke in Moroccan Patients.

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

Mutational analysis of the RB1 gene in Moroccan patients with retinoblastoma

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

TNF A -308G>A polymorphism in Moroccan patients with type 2 diabetes mellitus: a case-control study and meta-analysis

The Moroccan Genetic Disease Database (MGDD): a database for DNA variations related to inherited disorders and disease susceptibility

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

The prevalence of resistance-associated mutations to protease and reverse transcriptase inhibitors in treatment-naïve (HIV1)-infected individuals in Casablanca, Morocco.

c.1643_1644delTG XPC mutation is more frequent in Moroccan patients with xeroderma pigmentosum.