1. Detecting copy number variation in the human genome using comparative genomic hybridization. (October 2006) Authors: Tchinda, Joëlle; Lee, Charles Journal: Biotechniques Issue: Volume 41:Number 4(2006) Page Start: 385 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Detection of rare reciprocal RUNX1 rearrangements by next‐generation sequencing in acute myeloid leukemia. Issue 4 (2nd December 2019) Authors: Flach, Johanna; Shumilov, Evgenii; Joncourt, Raphael; Porret, Naomi; Tchinda, Joëlle; Legros, Myriam; Scarpelli, Ilaria; Hewer, Ekkehard; Novak, Urban; Schoumans, Jacqueline; Bacher, Ulrike; Pabst, Thomas Journal: Genes, chromosomes & cancer Issue: Volume 59:Issue 4(2020) Page Start: 268 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Microarray‐based comparative genomic hybridisation reveals additional recurrent aberrations in adult patients evaluated for myelodysplastic syndrome with normal karyotype. (9th January 2018) Authors: Ouahchi, Ines; Zhang, Luduo; Benitez Brito, Ramon; Benz, Rudolf; Müller, Rouven; Bonadies, Nicolas; Tchinda, Joëlle Journal: British journal of haematology Issue: Volume 184:Number 2(2019) Page Start: 282 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Myoepithelial Carcinoma of Soft Tissue With an EWSR1-KLF15 Gene Fusion in an Infant. (August 2021) Authors: Bodis, Sandor; Kroiss, Sabine; Tchinda, Joëlle; Fritz, Christine; Wagner, Ulrich; Bode, Peter Karl Journal: Pediatric and developmental pathology Issue: Volume 24:Number 4(2021) Page Start: 371 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗