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Publications by Laurence Faivre

Morphology and Genomic Hallmarks of Breast Tumours Developed by ATM Deleterious Variant Carriers

Breast Cancer Research

Cancer Research

English

Heterozygous Deletion of the LRFN2 Gene Is Associated With Working Memory Deficits

European Journal of Human Genetics

English

Altered Chemotactic Response to CXCL12 in Patients Carrying GATA2 Mutations

Journal of Leukocyte Biology

English

Molecular Study of the Perforin Gene in Familial Hematological Malignancies

Hereditary Cancer in Clinical Practice

English

TheFBN2gene: New Mutations, Locus-Specific Database (Universal Mutation DatabaseFBN2), and Genotype-Phenotype Correlations

English

Whole Mitochondrial Genome Screening in Maternally Inherited Non-Syndromic Hearing Impairment Using a Microarray Resequencing Mitochondrial DNA Chip

European Journal of Human Genetics

English

BBS8 Is Rarely Mutated in a Cohort of 128 Bardet–Biedl Syndrome Families

Journal of Human Genetics

English

Des Mutations Dans L’exonHSN2du gèneWNK1causent La Neuropathie Héréditaire Sensitive Et Autonomique De Type 2

Medecine/Sciences

Molecular Biology

English