Loss of TOP3B leads to increased R-loop formation and genome instability von Zhang, Tao, Wallis, Mathew, Petrovic, Vida, Challis, Jackie, Kalitsis, Paul, Hudson, Damien F

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Investigation of perinatal chromosomal mosaicism – using evidence to inform best practice von Burgess, Amber, Casey, Ellen, Williams, Lorna, Francis, David, Petrovic, Vida, Flowers, Nicola, Pertile, Mark, Lunke, Sebastian, Wall, Meg

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Comparing saliva and blood for the detection of mosaic genomic abnormalities that cause syndromic intellectual disability von Francis, David I, Stark, Zornitza, Scheffer, Ingrid E, Tan, Tiong Yang, Murali, Krithika, Gallacher, Lyndon, Amor, David J, Goel, Himanshu, Downie, Lilian, Stutterd, Chloe A, Krzesinski, Emma I, Vasudevan, Anand, Oertel, Ralph, Petrovic, Vida, Boys, Amber, Wei, Vivian, Burgess, Trent, Dun, Karen, Oliver, Karen L, Baxter, Anne, Hackett, Anna, Ayres, Samantha, Lunke, Sebastian, Kalitsis, Paul, Wall, Meaghan

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Intellectual Disability Gene Discovery In a Diagnostic Setting von Boys, Amber, Francis, David, Petrovic, Vida, Saddin, Simon, Tan, Tiong, Lunke, Sebastian

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Molecular mapping of the putative gonadoblastoma locus on the Y chromosome von Salo, Pia, Kääriäinen, Helena, Petrovic, Vida, Peltomäki, Päivi, Page, David C., de la Chapelle, Albert

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The application of RNA sequencing for the diagnosis and genomic classification of pediatric acute lymphoblastic leukemia von Brown, Lauren M., Lonsdale, Andrew, Zhu, Andrea, Davidson, Nadia M., Schmidt, Breon, Hawkins, Anthony, Wallach, Elise, Martin, Michelle, Mechinaud, Francoise M., Khaw, Seong Lin, Bartolo, Ray C., Ludlow, Louise E.A., Challis, Jackie, Brooks, Ian, Petrovic, Vida, Venn, Nicola C., Sutton, Rosemary, Majewski, Ian J., Oshlack, Alicia, Ekert, Paul G.

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Targeted therapy and disease monitoring in CNTRL‐FGFR1‐driven leukaemia von Brown, Lauren M., Bartolo, Ray C., Davidson, Nadia M., Schmidt, Breon, Brooks, Ian, Challis, Jackie, Petrovic, Vida, Khuong‐Quang, Dong‐Anh, Mechinaud, Francoise, Khaw, Seong L., Majewski, Ian J., Oshlack, Alicia, Ekert, Paul G.

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Use of ubiquitous, highly heterozygous copy number variants and digital droplet polymerase chain reaction to monitor chimerism after allogeneic haematopoietic stem cell transplanta... von Whitlam, John B, Ling, Ling, Swain, Michael, Harrington, Tom, Mirochnik, Oksana, Brooks, Ian, Cronin, Sara, Challis, Jackie, Petrovic, Vida, Bruno, Damien L, Mechinaud, Francoise, Conyers, Rachel, Slater, Howard

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Low grade fibromyxoid sarcoma: problems in the diagnosis and management of a malignant tumour with bland histological appearance von Wu, Xiangru, Petrovic, Vida, Torode, Ian P., Chow, Chung Wo

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A functional marker centromere with no detectable alpha-satellite, satellite III, or CENP-B protein : activation of a latent centromere ? von VOULLAIRE, L. E, SLATER, H. R, PETROVIC, V, ANDY CHOO, K. H

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Length of procedure as a cause of damage von Petrovic-Skero, Vida

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Directly inherited partial trisomy of chromosome 6p identified in a father and daughter by chromosome microdissection von Delatycki, Martin B, Voullaire, Lucille, Francis, David, Petrovic, Vida, Robertson, Anne, Webber, Lorna M, Slater, Howard R

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Expansion of the CGG repeat in fragile X in the FMRI gene depends on the sex of the offspring von LOESCH, D. Z, HUGGINS, R, PETROVIC, V, SLATER, H

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PRENATAL DIAGNOSIS OF PRADER-WILLI SYNDROME USING PW71 METHYLATION ANALYSIS-UNIPARENTAL DISOMY AND THE SIGNIFICANCE OF RESIDUAL TRISOMY 15 von SLATER, HOWARD R., VAUX, CATHRYN, PERTILE, MARK, BURGESS, TRENT, PETROVIC, VIDA

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"Reduction" of CGG trinucleotide expansion from mother to offspring in seven fragile-X families von Loesch, Danuta Z., Petrovic, Vida, Francis, David I., Oertel, Ralph, Slater, Howard

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Studiranje i izdržavanje von Petrović-Škero, Vida

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Complex CGH alterations on chromosome arm 8p at candidate tumor suppressor gene loci in breast cancer cell lines von Venter, Deon J., Ramus, Susan J., Hammet, Fleur M.A., de Silva, Melanie, Hutchins, Anne-Marie, Petrovic, Vida, Price, Gareth, Armes, Jane E.

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X chromosome inactivation in fibroblasts of mentally retarded female carriers of the fragile site Xq27.3: Application of the probe M27β to evaluate X inactivation status von Schmidt, Malgorzata, Du Sart, Desirée, Kalitsis, Paul, Fraser, Neil, Leversha, Margaret, Voullaire, Lucille, Foster, Dean, Davies, Julie, Hills, Louise, Petrovic, Vida, Hutchinson, Rhonda

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The high judicial council status, election, dismissal, mandate, participation, jurisdiction von Petrović-Škero, Vida

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Cytogenetic and DNA analysis of two neuroectodermal tumors without a simple t(11;22) von Slater, Howard R., Tiong, Tak, Konstantakopoulos, Sophia, Sham, Connie, Petrovic, Vida, Voullaire, Lucille, Kannourakis, George

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