Lista de obras -

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 of 15 autosomal STR loci in the southern Morocco population with phylogenetic structure among worldwide populations

artículo científico publicado en 2009

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

Assessment of phylogenetic structure of Berber-speaking population of Azrou using 15 STRs of Identifiler kit.

artículo científico publicado en 2009

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

artículo científico publicado en 2008

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 polymorphism in the manganese superoxide dismutase gene is associated with an increased risk for hepatocellular carcinoma in HCV-infected Moroccan patients

artículo científico publicado en 2007

Genotype determination in Moroccan hepatitis B chronic carriers.

artículo científico publicado en 2008

Male sterility thermal thresholds in Drosophila: D. simulans appears more cold-adapted than its sibling D. melanogaster.

artículo científico publicado en 2002

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

artículo científico publicado en 2008

Novel mutations involving the INSL3 gene associated with cryptorchidism

artículo científico publicado en 2007

Phenotypic plasticity of adult size and pigmentation in Drosophila: thermosensitive periods during development in two sibling species

artículo científico publicado en 2002

Prevalence of common HFE and SERPINA1 mutations in patients with hepatocellular carcinoma in a Moroccan population

artículo científico publicado en 2008

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

artículo científico publicado en 2010

The Pro variant of the p53 codon 72 polymorphism is associated with hepatocellular carcinoma in Moroccan population

artículo científico publicado en 2007

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

Lista de obras de

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 of 15 autosomal STR loci in the southern Morocco population with phylogenetic structure among worldwide populations

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

Assessment of phylogenetic structure of Berber-speaking population of Azrou using 15 STRs of Identifiler kit.

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

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 polymorphism in the manganese superoxide dismutase gene is associated with an increased risk for hepatocellular carcinoma in HCV-infected Moroccan patients

Genotype determination in Moroccan hepatitis B chronic carriers.

Male sterility thermal thresholds in Drosophila: D. simulans appears more cold-adapted than its sibling D. melanogaster.

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

Novel mutations involving the INSL3 gene associated with cryptorchidism

Phenotypic plasticity of adult size and pigmentation in Drosophila: thermosensitive periods during development in two sibling species

Prevalence of common HFE and SERPINA1 mutations in patients with hepatocellular carcinoma in a Moroccan population

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

The Pro variant of the p53 codon 72 polymorphism is associated with hepatocellular carcinoma in Moroccan population

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