1. Directly inherited partial trisomy of chromosome 6p identified in a father and daughter by chromosome microdissection. Issue 4 (1st April 1999) Authors: Delatycki, Martin B; Voullaire, Lucille; Francis, David; Petrovic, Vida; Robertson, Anne; Webber, Lorna M; Slater, Howard R Journal: Journal of medical genetics Issue: Volume 36:Issue 4(1999) Page Start: 335 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Early Detection of Fragile X Syndrome: Applications of a Novel Approach for Improved Quantitative Methylation Analysis in Venous Blood and Newborn Blood Spots. (1st July 2014) Authors: Inaba, Yoshimi; Schwartz, Charles E; Bui, Quang M; Li, Xin; Skinner, Cindy; Field, Michael; Wotton, Tiffany; Hagerman, Randi J; Francis, David; Amor, David J; Hopper, John L; Loesch, Danuta Z; Bretherton, Lesley; Slater, Howard R; Godler, David E Journal: Clinical chemistry Issue: Volume 60:Number 7(2014) Page Start: 963 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Further molecular and clinical delineation of co-locating 17p13.3 microdeletions and microduplications that show distinctive phenotypes. Issue 5 (7th May 2010) Authors: Bruno, Damien L; Anderlid, Britt-Marie; Lindstrand, Anna; van Ravenswaaij-Arts, Conny; Ganesamoorthy, Devika; Lundin, Johanna; Martin, Christa Lese; Douglas, Jessica; Nowak, Catherine; Adam, Margaret P; Kooy, R Frank; Van der Aa, Nathalie; Reyniers, Edwin; Vandeweyer, Geert; Stolte-Dijkstra, Iren... Journal: Journal of medical genetics Issue: Volume 47:Issue 5(2010) Page Start: 299 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Identification of Males with Cryptic Fragile X Alleles by Methylation-Specific Quantitative Melt Analysis. (6th January 2020) Authors: Aliaga, Solange M; Slater, Howard R; Francis, David; Du Sart, Desiree; Li, Xin; Amor, David J; Alliende, Angelica M; Santa Maria, Lorena; Faundes, Víctor; Morales, Paulina; Trigo, Cesar; Salas, Isabel; Curotto, Bianca; Godler, David E Journal: Clinical chemistry Issue: Volume 62:Number 2(2016) Page Start: 343 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Neocentromere formation in a stable ring 1p32-p36.1 chromosome. Issue 12 (1st December 1999) Authors: Slater, Howard R; Nouri, Sara; Earle, Elizabeth; Lo, Anthony W I; Hale, Lyndon G; Choo, K H Andy Journal: Journal of medical genetics Issue: Volume 36:Issue 12(1999) Page Start: 914 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Use of Copy Number Deletion Polymorphisms to Assess DNA Chimerism. (1st August 2014) Authors: Bruno, Damien L; Ganesamoorthy, Devika; Thorne, Natalie P; Ling, Ling; Bahlo, Melanie; Forrest, Sue; Veenendaal, Marieke; Katerelos, Marina; Skene, Alison; Ierino, Frank L; Power, David A; Slater, Howard R Journal: Clinical chemistry Issue: Volume 60:Number 8(2014) Page Start: 1105 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗