Bienvenu, Thierry, 19..-....
VIAF ID: 308302396 (Personal)
Permalink: http://viaf.org/viaf/308302396
Preferred Forms
Works
Title | Sources |
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Architecture génétique des troubles du spectre autistique dans les îles Féroé | |
DNA Methylation is altered in cystic fibrosis nasal epithelial and blood cells. | |
Elevated levels of the adipocyte hormone leptin contribute to Rett syndrome associated symptoms in male Mecp2-null mice. | |
Epigenetic regulation of CFTR gene. | |
Etude de la contribution de l'hormone adipocytaire leptine dans la pathogenèse du syndrome de Rett | |
Exploration of the pathophysiological mechanisms underlying Rett syndrome. | |
The Genetic Architecture of Autism Spectrum Disorders in the Faroe Islands. | |
Genetic bases of anorexia nervosa in males : identification of a candidate gene encoding neuronatin. | |
HETEROGENEITE DES MUTATIONS ET COMPLEXITE DE L'EPISSAGE DU GENE CFTR : RELATION AVEC LA VARIABILITE CLINIQUE DE LA MUCOVISCIDOSE | |
Identifying candidate genes predisposing to hereditary spinocerebellar degeneration in a cohort of Sudanese families | |
La méthylation de l'ADN est altérée dans les cellules nasales et sanguines des patients atteints de mucoviscidose | |
Les microtubules, cibles potentielles pour le traitement du syndrome de Rett | |
Mutations heterogeneity and complexity of the splicing pattern in the cftr gene: correlations with the variable phenotype of the cystic fibrosis. | |
Retards mentaux syndromiques et anomalies moléculaires de ZEB2 : nouveaux spectres clinico-biologiques | |
Syndromic intellectual disabilities and ZEB2 anomalies. |