R. Fetni

Whole‐genome array CGH identifies pathogenic copy number variations in fetuses with major malformations and a normal karyotype

E. Lemyre, V. Désilets, J. Michaud, 2012, Clinical genetics.

Frequency of Chromosome Healing and Interstitial Telomeres in 40 Cases of Constitutional Abnormalities

Raouf Fetni, N. Lemieux, M. Beaulieu Bergeron, 2009, Cytogenetic and Genome Research.

SNP arrays: comparing diagnostic yields for four platforms in children with developmental delay

E. Lemyre, M. Srour, G. Mathonnet, 2014, BMC Medical Genomics.

SNP genotyping of a sclerosing rhabdomyosarcoma: reveals highly aneuploid profile and a specific MDM2/HMGA2 amplification.

A. Montpetit, A. Rougemont, D. Bouron‐Dal Soglio, 2009, Human pathology.

A t(17;22)(q21;q12) with partial ETV4 deletion in a soft tissue Ewing sarcoma.

A. Rougemont, D. Bouron‐Dal Soglio, J. Fournet, 2012, Cancer genetics.

Chondroid Cystic Malformation of the Lung With Trisomy 8 Mosaicism: A New Cystic Lung Malformation

A. Montpetit, A. Rougemont, D. Bouron‐Dal Soglio, 2008, The American journal of surgical pathology.