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	1.	Down syndrome with apparently normal chromosomes: an update. [electronic resource] by Kirkilionis, A J Sergovich, F R Producer: 19860616 In: The Journal of pediatrics vol. 108 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Supernumary marker chromosomes in a mentally retarded population identified as inv dup(15). [electronic resource] by Kirkilionis, A J Sergovich, F R Producer: 19870930 In: Clinical genetics vol. 31 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	The use of testicular volume as a clinical marker for cytogenetic disorders in mentally retarded males. [electronic resource] by Kirkilionis, A J Pozsonyi, J Sergovich, F R Producer: 19880602 In: Journal of mental deficiency research vol. 32 ( Pt 1) Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Long-range restriction mapping and linkage analysis of the Prader-Willi chromosome region (PWCR). [electronic resource] by Kirkilionis, A J Gregory, C A Hamerton, J L Producer: 19910625 In: Genomics vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Prenatal diagnosis of 45,X/46,XY mosaicism in a fetus with asymmetric gonadal dysgenesis. [electronic resource] by Kirkilionis, A J Rodney, P Sergovich, F R Armstrong, R Producer: 19871130 In: Prenatal diagnosis vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Fabry disease in a large Nova Scotia kindred: carrier detection using leucocyte alpha-galactosidase activity and an NcoI polymorphism detected by an alpha-galactosidase cDNA clone. [electronic resource] by Kirkilionis, A J Riddell, D C Spence, M W Fenwick, R G Producer: 19910828 In: Journal of medical genetics vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Molecular and clinical overlap of Angelman and Prader-Willi syndrome phenotypes. [electronic resource] by Kirkilionis, A J Chudley, A E Gregory, C A Hamerton, J L Producer: 19920115 In: American journal of medical genetics vol. 40 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Somatic recombination rather than uniparental disomy suggested as another mechanism by which genetic imprinting may play a role in the etiology of Prader-Willi syndrome. [electronic resource] by Gregory, C A Schwartz, J Kirkilionis, A J Rudd, N Hamerton, J L Producer: 19920103 In: Human genetics vol. 88 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Detection of molecular rearrangements in Prader-Willi syndrome patients by using genomic probes recognizing four loci within the PWCR. [electronic resource] by Gregory, C A Kirkilionis, A J Greenberg, C R Chudley, A E Hamerton, J L Producer: 19900607 In: American journal of medical genetics vol. 35 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Transmission of the fra(X) haplotype from three nonpenetrant brothers to their affected grandsons. [electronic resource] by Kirkilionis, A J Chudley, A E Greenberg, C R Yan, D L McGillivray, B Hamerton, J L Producer: 19920716 In: American journal of medical genetics vol. 43 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)