Siobhan Battersby, Praveen Sharma, Dorothy Hung, Luke St Heaps, Dale Wright Sydney Genome Diagnostics, Children’s Hospital at Westmead, NSW, Australia Background: The recurrent t(8;21) abnormality found in primary acute myeloid leukaemia (AML) is associated with a favourable prognosis. In therapy-related...
- February 15, 2017
El-Hajj Racha, St. Heaps Luke, Clark Alissa and Wright Dale. Sydney Genome Diagnostics, Cytogenetic Department, The Children’s Hospital at Westmead, NSW, Australia. Background Multiple myeloma (MM) is a plasma cell (PC) neoplasm in which the surface antigen CD138 (syndecan-1) is highly...
- February 15, 2017
Mahony Fenn1, Ryan Hedley1, Dr. Melody Caramins2, Dr. Nicole Chia3 1 Western Diagnostic Pathology, 74 McCoy St, Myaree, WA, 6154, Mahony.Fenn@wdp.com.au 2 Genomic Diagnostics, 60 Waterloo Road, Macquarie Park, NSW, 2113 3 Queensland Medical Laboraory, Metroplex on Gateway, 11 Riverview...
- February 15, 2017
Shravan K Yellenki, Mioara Gavrila, Elizabeth M Algar Genetics and Molecular Pathology, Monash Health, 246 Clayton Rd, Clayton, VICTORIA 1 in 3 Australian men and 1 in 4 Australian women will be diagnosed with cancer before the age of 75....
- February 15, 2017
Dannielle Ghezzi1, Khoa Lam1, Wendy Waters2, Sarah Smith2, Enzo Ranieri1, Dr Michael Metz1, Dr Janice Fletcher1, Peter Sharp3 1 Antenatal Screening Laboratory , Department of Biochemical Genetics, Directorate of Genetics & Molecular Pathology, SA Pathology, Women’s and Children’s Hospital,...
- February 15, 2017
Wendy M Hutchison1, Kerryn M Weekes1, Jeremy N Wells1, Ruoxin Li1, Nicholas Clark1, Anita Feigin2,3, Asif Alam1, Elizabeth Algar4, Zane Kaplan2 1 Thalassaemia & Haemophilia Molecular Reference Laboratory, Level 3 Monash Medical Centre 246 Clayton Road, CLAYTON, VIC, 3168, wendy.hutchison@monashhealth.org...
- February 15, 2017
Sharanbeer Kaur, Gregory Peters, Dale Wright Sydney Genome Diagnostics, The Children’s Hospital Westmead, NSW, 2145 Introduction: The recurrent 3q13.2q31.31 microdeletion has been associated with a rare but emerging syndrome with clinical features overlapping Primrose syndrome. Herein, two cases are...
- February 15, 2017
Louise Korte1, Sarah Higgins1, Jillian Nicholl1, Alison Attwood1, Ryan Storer1, Sarah Smith1, Yvonne Hull1, Sue Brown1, Rhonda Hutchinson1, Christopher Barnett2, Jan Liebelt2 1SA Pathology, Cytogenetics Unit, Department of Genetic Medicine, WCH, 72 King William Road, North Adelaide, SA, 5006 2SA...
- February 15, 2017
Vanessa McLaughlin1, Paula Lall1, Louise Hills1, Sorour Voghoei1, Dao Nguyen1, Michael Cronin1, Amber Boys1, Fiona Norris1, David Francis1, Martin Delatycki1 1VCGS, Level 4 MCRI Building, Royal Children’s Hospital, Flemington Rd, Parkville, 3052 Microarray analysis and FISH testing were requested on...
- February 15, 2017
Holly Napret, Dean Grimmond, Artur Darmanian and Dale Wright 1Sydney Genome Diagnostics, The Children’s Hospital at Westmead, Hawkesbury Rd, Westmead NSW 2145 Background: The 22q11.2 region is complex with well-defined segmental duplications, or low copy repeats (LCR), which predispose...
- February 15, 2017
