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1. Cryptic recurrent ACIN1‐NUTM1 fusions in non‐KMT2A‐rearranged infant acute lymphoblastic leukemia. Issue 2 (4th October 2019)

2. Genomic study of severe fetal anomalies and discovery of GREB1L mutations in renal agenesis. (July 2018)

3. LINE‐ and Alu‐containing genomic instability hotspot at 16q24.1 associated with recurrent and nonrecurrent CNV deletions causative for ACDMPV. Issue 12 (22nd August 2018)

5. Prenatal presentation of glutaric aciduria type II: A case report with radiologic, clinical, biochemical, molecular, and pathological phenotyping. Issue 3 (12th January 2021)