A. Chafik

发表

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

H. Rouba, A. Barakat, Redouane Boulouiz, 2008, International journal of pediatric otorhinolaryngology.

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

P. Pineau, S. Benjelloun, S. Ezzikouri, 2008, Archives of medical research.

Digital dermatoglyphic patterns of Moroccan Arabs: relationships with Mediterranean populations.

P. Moral, A. Chafik, M. Kandil, 1998, Annals of human biology.

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

H. Bolz, Yun Li, B. Wollnik, 2007, Molecular vision.

No Association between T222P/LGR8 Mutation and Cryptorchidism in the Moroccan Population

H. Rouba, A. Barakat, K. McElreavey, 2008, Hormone Research in Paediatrics.

Genotype determination in Moroccan hepatitis B chronic carriers.

P. Pineau, A. Dejean, I. Chemin, 2008, Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases.

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

H. Rouba, A. Barakat, K. McElreavey, 2007, Asian journal of andrology.

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

P. Pineau, S. Benjelloun, S. Ezzikouri, 2007, Hepatology research : the official journal of the Japan Society of Hepatology.

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

B. Bouchrif, A. Chafik, D. Zaoui, 2010, Legal medicine.

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

B. Bouchrif, A. Chafik, Jalal Talbi, 2009, Legal medicine.

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

H. Rouba, A. Barakat, Redouane Boulouiz, 2007, International journal of pediatric otorhinolaryngology.

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

H. Rouba, A. Barakat, Redouane Boulouiz, 2008, Biochemical and biophysical research communications.

Heterosis retained in different generations of inter se mating between D’man and Sardi sheep

A. Chafik, By I. Boujenane, M. Benbihi, 1999 .

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

J. David, M. Chakir, P. Gibert, 2002 .

Male Sterility Thermal Thresholds in Drosophila: D. simulans Appears More Cold-adapted Than its Sibling D. melanogaster

J. David, M. Chakir, B. Moréteau, 2002, Genetica.

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

G. Nürnberg, C. Becker, P. Nürnberg, 2008, American journal of medical genetics. Part A.

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

P. Pineau, S. Benjelloun, S. Ezzikouri, 2008, Mutation research.

Apolipoprotein molecular variation in Moroccan Berbers: pentanucleotide (TTTTA)n repeat in the LPA gene and APOE‐C1‐C2 gene cluster

P. Moral, E. Esteban, A. López-Alomar, 2002, Clinical genetics.

Classical polymorphisms in Berbers from Moyen Atlas (Morocco): genetics, geography, and historical evidence in the Mediterranean peoples

P. Moral, G. Vona, E. Esteban, 2002, Annals of human biology.

Dermatoglyphic characterization of Berbers from Morocco: qualitative and quantitative digital and palm data

P. Moral, E. Esteban, N. Harich, 2002, Annals of human biology.

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

H. Benrahma, H. Rouba, A. Barakat, 2010, International journal of pediatric otorhinolaryngology.

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

H. Rouba, A. Barakat, Redouane Boulouiz, 2008, Genetic testing.

Mutations in the protamine locus: association with spermatogenic failure?

H. Rouba, A. Barakat, K. McElreavey, 2009, Molecular human reproduction.

Novel mutations involving the INSL3 gene associated with cryptorchidism.

H. Rouba, A. Barakat, K. McElreavey, 2007, The Journal of urology.