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	1.	Chromosome loops arising from intrachromosomal tethering of telomeres occur at high frequency in G1 (non-cycling) mitotic cells: Implications for telomere capture. [electronic resource] by Daniel, Art St Heaps, Luke Publication details: Cell & chromosome Sep 2004 In: Cell & chromosome vol. 3 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Apparently unrelated cytogenetic abnormalities among 462 probands referred for the detection of del(22q) by FISH. [electronic resource] by Smith, Arabella St Heaps, Luke Robson, Lisa Producer: 20031003 In: American journal of medical genetics vol. 113 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Use of two FISH probes provides a cost-effective, simple protocol to exclude an imprinting centre defect in routine laboratory testing for suspected Prader-Willi and Angelman syndrome. [electronic resource] by Smith, Arabella Robson, Lisa St Heaps, Luke Producer: 20031103 In: Annales de genetique vol. 45 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Two mosaic terminal inverted duplications arising post-zygotically: Evidence for possible formation of neo-telomeres. [electronic resource] by Daniel, Art St Heaps, Luke Sylvester, Dianne Diaz, Sara Peters, Gregory Producer: 20110714 In: Cell & chromosome vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Use of FISH in an aggressive diffuse large B cell lymphoma. [electronic resource] by Smith, Arabella Kirkpatrick, Philippa St Heaps, Luke Sharma, Praveen Roman, Marcella Harvey, Theresa Crombie, Catherine Producer: 20031016 In: Pathology vol. 35 Availability: No items available. Save to lists Add to cart (remove)
	6.	A balanced paternal interchromosomal reciprocal insertion between 5q12.1q13.2 and 20p12.3p12.1 resulting in separate genetic conditions in two siblings. [electronic resource] by Wallis, Mathew J Kelly, Amanda L Peters, Gregory B St Heaps, Luke Nandini, Adayapalam McGaughran, Julie M Producer: 20180129 In: American journal of medical genetics. Part A vol. 170 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Paternally inherited submicroscopic duplication at 11p15.5 implicates insulin-like growth factor II in overgrowth and Wilms' tumorigenesis. [electronic resource] by Algar, Elizabeth M St Heaps, Luke Darmanian, Artur Dagar, Vinod Prawitt, Dirk Peters, Greg B Collins, Felicity Producer: 20070412 In: Cancer research vol. 67 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	A Paediatric Acute Promyelocytic Leukaemia Patient Harbouring a Cryptic PML-RARA Insertion due to a Complex Structural Chromosome 17 Rearrangement. [electronic resource] by El-Hajj Ghaoui, Racha St Heaps, Luke Hung, Dorothy Nagabushan, Sumanth Harris, Catherine Mirochnik, Oksana Sharma, Praveen Kellie, Stewart J Wright, Dale C Producer: 20180405 In: Cytogenetic and genome research vol. 153 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Three patients with terminal deletions within the subtelomeric region of chromosome 9q. [electronic resource] by Neas, Katherine R Smith, Janine M Chia, Nicole Huseyin, Suna St Heaps, Luke Peters, Greg Sholler, Gary Tzioumi, Dimitra Sillence, David O Mowat, David Producer: 20050418 In: American journal of medical genetics. Part A vol. 132A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Axenfeld-Rieger malformation and distinctive facial features: Clues to a recognizable 6p25 microdeletion syndrome. [electronic resource] by Maclean, Kenneth Smith, James St Heaps, Luke Chia, Nicole Williams, Rebecca Peters, Gregory B Onikul, Ella McCrossin, Tim Lehmann, Ordan J Adès, Lesley C Producer: 20050418 In: American journal of medical genetics. Part A vol. 132A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Chromosomal rearrangements and novel genes in disorders of eye development, cataract and glaucoma. [electronic resource] by Mihelec, Marija St Heaps, Luke Flaherty, Maree Billson, Frank Rudduck, Christina Tam, Patrick P L Grigg, John R Peters, Greg B Jamieson, Robyn V Producer: 20090113 In: Twin research and human genetics : the official journal of the International Society for Twin Studies vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Deletion at 14q22-23 indicates a contiguous gene syndrome comprising anophthalmia, pituitary hypoplasia, and ear anomalies. [electronic resource] by Nolen, Leisha D Amor, David Haywood, Ashley St Heaps, Luke Willcock, Chris Mihelec, Marija Tam, Patrick Billson, Frank Grigg, John Peters, Greg Jamieson, Robyn V Producer: 20060928 In: American journal of medical genetics. Part A vol. 140 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Tumor protein D52 (TPD52) is overexpressed and a gene amplification target in ovarian cancer. [electronic resource] by Byrne, Jennifer A Balleine, Rosemary L Schoenberg Fejzo, Marlena Mercieca, Janelle Chiew, Yoke-Eng Livnat, Yael St Heaps, Luke Peters, Gregory B Byth, Karen Karlan, Beth Y Slamon, Dennis J Harnett, Paul Defazio, Anna Producer: 20051214 In: International journal of cancer vol. 117 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)