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	1.	Three cases of dup(10p)/del(10q) syndrome resulting from maternal pericentric inversion. [electronic resource] by Kulharya, A S Schneider, N R Wilson, G N Producer: 19940204 In: American journal of medical genetics vol. 47 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Trisomy 22: no longer an enigma. [electronic resource] by Kukolich, M K Kulharya, A Jalal, S M Drummond-Borg, M Producer: 19900323 In: American journal of medical genetics vol. 34 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Maternal complex chromosome rearrangement ascertained through a del (13)(q12.1q14.1) detected in her mildly affected daughter. [electronic resource] by Drummond-Borg, M Kulharya, A S Tonk, V Garcia-Heras, J Producer: 20020306 In: American journal of medical genetics vol. 107 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Constitutional del(19)(q12q13.1) in a three-year-old girl with severe phenotypic abnormalities affecting multiple organ systems. [electronic resource] by Kulharya, A S Michaelis, R C Norris, K S Taylor, H A Garcia-Heras, J Producer: 19990205 In: American journal of medical genetics vol. 77 Availability: No items available. Save to lists Add to cart (remove)
	5.	Prenatal diagnosis of a trisomy 17p derived from a de novo non-mosaic satellited marker. [electronic resource] by Kulharya, A S Garcia-Heras, J Radtke, H B Norris, K S Keppen, L D Flannery, D B Producer: 19990205 In: Clinical genetics vol. 54 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Mild phenotypic effects of a de novo deletion Xpter-->Xp22.3 and duplication 3pter-->3p23. [electronic resource] by Kulharya, A S Roop, H Kukolich, M K Nachtman, R G Belmont, J W Garcia-Heras, J Producer: 19950613 In: American journal of medical genetics vol. 56 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Packed red cell transfusion does not compromise chromosome analysis in newborns. [electronic resource] by Kulharya, A S Salbert, B A Norris, K N Cook, L Larrison, P J Flannery, D B Producer: 20020201 In: Genetics in medicine : official journal of the American College of Medical Genetics vol. 3 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Radiation therapy depletes extrachromosomally amplified drug resistance genes and oncogenes from tumor cells via micronuclear capture of episomes and double minute chromosomes. [electronic resource] by Schoenlein, Patricia V Barrett, John T Kulharya, A Dohn, Michael R Sanchez, Ana Hou, D-Y McCoy, J Producer: 20030403 In: International journal of radiation oncology, biology, physics vol. 55 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Interstitial deletions 4q21.1q25 and 4q25q27: phenotypic variability and relation to Rieger anomaly. [electronic resource] by Kulharya, A S Maberry, M Kukolich, M K Day, D W Schneider, N R Wilson, G N Tonk, V Producer: 19950512 In: American journal of medical genetics vol. 55 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Kenny-Caffey syndrome and microorchidism. [electronic resource] by Hoffman, W H Kovacs, K Li, S Kulharya, A S Johnson, B L Eidson, M S Cleveland, W W Producer: 19990107 In: American journal of medical genetics vol. 80 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Exclusion of SIX6 hemizygosity in a child with anophthalmia, panhypopituitarism and renal failure. [electronic resource] by Rauchman, M Hoffman, W H Hanna, J D Kulharya, A S Figueroa, R E Yang, J Tuck-Miller, C M Producer: 20020221 In: American journal of medical genetics vol. 104 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Prenatal diagnosis of a de novo trisomy 6q22.2-->6qter and monosomy 1pter-->1p36.3. Case report with a 2-year follow-up and a brief review of other prenatal cases of partial trisomy 6q. [electronic resource] by Kulharya, A S Carlin, M E Stettler, R W Huslig, M Kukolich, M K Garcia-Heras, J Stettler, W A Producer: 19970619 In: Clinical genetics vol. 51 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)