Lista de obras - Hicham Charoute - Dominio Público Uruguay

A Novel Homozygous Missense Mutation in the FU-CRD2 Domain of the R-spondin1 Gene Associated with Familial 46,XX DSD.

artículo científico publicado en 2017

A novel mutation in SLITRK6 causes deafness and myopia in a Moroccan family.

artículo científico publicado en 2018

A novel mutation in the TMC1 gene causes non-syndromic hearing loss in a Moroccan family.

artículo científico publicado en 2015

Association analysis of APOA5 rs662799 and rs3135506 polymorphisms with obesity in Moroccan patients.

artículo científico publicado en 2015

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

Association analysis of genetic variants with metabolic syndrome components in the Moroccan population

artículo científico publicado en 2017

Association of APOA5 rs662799 and rs3135506 polymorphisms with arterial hypertension in Moroccan patients.

artículo científico publicado en 2014

Association study of HNF1A polymorphisms with metabolic syndrome in the Moroccan population

artículo científico publicado en 2017

Chromosomal abnormalities and Y chromosome microdeletions in infertile men from Morocco

artículo científico publicado en 2015

Compound heterozygous SLC29A3 mutation causes H syndrome in a Moroccan patient: A case report.

artículo científico publicado en 2016

Computational Analysis of the Potential Impact of MTC Complex Missenses SNPs Associated with Male Infertility

artículo científico publicado en 2022

Haplotype analysis of the Apolipoprotein A5 gene in Moroccan patients with the metabolic syndrome

artículo científico publicado en 2015

Homozygous mutations in PJVK and MYO15A genes associated with non-syndromic hearing loss in Moroccan families.

artículo científico publicado en 2017

Intra-familial phenotypic variability in a Moroccan family with hearing loss and palmoplantar keratoderma (PPK).

artículo científico publicado en 2016

Mediterranean Founder Mutation Database (MFMD): Taking Advantage from Founder Mutations in Genetics Diagnosis, Genetic Diversity and Migration History of the Mediterranean Population

artículo científico publicado en 2015

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

artículo científico publicado en 2017

Novel compound heterozygous mutations in the GPR98 (USH2C) gene identified by whole exome sequencing in a Moroccan deaf family.

artículo científico publicado en 2017

Novel variants of mitochondrial DNA associated with Type 2 diabetes mellitus in Moroccan population

artículo científico publicado en 2016

Prediction of the Impact of Deleterious Nonsynonymous Single Nucleotide Polymorphisms on the Human RRM2B Gene: A Molecular Modeling Study

scientific article published on 25 July 2020

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

Lista de obras de Hicham Charoute

A Novel Homozygous Missense Mutation in the FU-CRD2 Domain of the R-spondin1 Gene Associated with Familial 46,XX DSD.

A novel mutation in SLITRK6 causes deafness and myopia in a Moroccan family.

A novel mutation in the TMC1 gene causes non-syndromic hearing loss in a Moroccan family.

Association analysis of APOA5 rs662799 and rs3135506 polymorphisms with obesity in Moroccan patients.

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

Association analysis of genetic variants with metabolic syndrome components in the Moroccan population

Association of APOA5 rs662799 and rs3135506 polymorphisms with arterial hypertension in Moroccan patients.

Association study of HNF1A polymorphisms with metabolic syndrome in the Moroccan population

Chromosomal abnormalities and Y chromosome microdeletions in infertile men from Morocco

Compound heterozygous SLC29A3 mutation causes H syndrome in a Moroccan patient: A case report.

Computational Analysis of the Potential Impact of MTC Complex Missenses SNPs Associated with Male Infertility

Haplotype analysis of the Apolipoprotein A5 gene in Moroccan patients with the metabolic syndrome

Homozygous mutations in PJVK and MYO15A genes associated with non-syndromic hearing loss in Moroccan families.

Intra-familial phenotypic variability in a Moroccan family with hearing loss and palmoplantar keratoderma (PPK).

Mediterranean Founder Mutation Database (MFMD): Taking Advantage from Founder Mutations in Genetics Diagnosis, Genetic Diversity and Migration History of the Mediterranean Population

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

Novel compound heterozygous mutations in the GPR98 (USH2C) gene identified by whole exome sequencing in a Moroccan deaf family.

Novel variants of mitochondrial DNA associated with Type 2 diabetes mellitus in Moroccan population

Prediction of the Impact of Deleterious Nonsynonymous Single Nucleotide Polymorphisms on the Human RRM2B Gene: A Molecular Modeling Study

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