Your search returned 28 results.

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	1.	Letter: Arterial occlusion in 47,XYY male. [electronic resource] by Kukolich, M Hall, J G Producer: 19751211 In: Lancet (London, England) vol. 2 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Endocardial fibroelastosis, neurologic dysfunction and unusual facial appearance in two brothers, coincidentally associated with dominantly inherited macrocephaly. [electronic resource] by Jennings, M T Hall, J G Kukolich, M Producer: 19801021 In: American journal of medical genetics vol. 5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Familial translocation leading to partial trisomy 13: report of three cases. [electronic resource] by Tharapel, S A Lewandowski, R C Kukolich, M K Producer: 19850408 In: Indian journal of pediatrics vol. 51 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Sudden infant death syndrome: normal QT interval on ECGs of relatives. [electronic resource] by Kukolich, M K Telsey, A Ott, J Motulsky, A G Producer: 19770812 In: Pediatrics vol. 60 Availability: No items available. Save to lists Add to cart (remove)
	5.	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)
	6.	Mosaic Down's syndrome with de novo 45,XX,-21,-22,+t(21q;22q)/46,XX,-21,+t(21q;21q) rearrangement. [electronic resource] by Tharapel, A T Redheendran, R Mankinen, C B Kukolich, M K Producer: 19850122 In: Journal of medical genetics vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Euchromatic 9q + heteromorphism in a family. [electronic resource] by Jalal, S M Kukolich, M K Garcia, M Day, D W Producer: 19901205 In: American journal of medical genetics vol. 37 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Hypomelanosis of Ito with triphalangeal thumbs. [electronic resource] by Kukolich, M K Althaus, B W Freeman, M V Lewandowski, R C Producer: 19800815 In: Journal of medical genetics vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Partial deletion 10q. [electronic resource] by Lewandowski, R C Kukolich, M K Sears, J W Mankinen, C B Producer: 19780930 In: Human genetics vol. 42 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Euchromatic 16p+ heteromorphism: first report in North America. [electronic resource] by Jalal, S M Schneider, N R Kukolich, M K Wilson, G N Producer: 19910125 In: American journal of medical genetics vol. 37 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Retinal pigment mosaicism in Pallister-Killian syndrome (mosaic tetrasomy 12p). [electronic resource] by Graham, W Brown, S M Shah, F Tonk, V S Kukolich, M K Producer: 19991221 In: Archives of ophthalmology (Chicago, Ill. : 1960) vol. 117 Availability: No items available. Save to lists Add to cart (remove)
	12.	Ring chromosome 8 syndrome: further characterization. [electronic resource] by Tonk, V S Kukolich, M K Morgan, D Khan, A Jalal, S M Producer: 20000315 In: American journal of medical genetics vol. 90 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Tetrasomy 9p: an emerging syndrome. [electronic resource] by Jalal, S M Kukolich, M K Garcia, M Benjamin, T R Day, D W Producer: 19910401 In: Clinical genetics vol. 39 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	Complete trisomy 17p a relatively new syndrome. [electronic resource] by Martsolf, J T Larson, L Jalal, S M Wasdahl, W A Miller, R Kukolich, M Producer: 19890322 In: Annales de genetique vol. 31 Availability: No items available. Save to lists Add to cart (remove)
	15.	Direct chromosome analysis from neonatal cord blood. [electronic resource] by Day, D W Jalal, S M Sinclair-Worley, L Kukolich, M Freeman, M Sakakini, J Producer: 19890505 In: American journal of medical genetics vol. 31 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	Abnormalities resulting from a familial pericentric inversion of chromosome 18. [electronic resource] by Kukolich, M K Althaus, B W Sears, J W Mankinen, C B Lewandowski, R C Producer: 19781122 In: Clinical genetics vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	Unusual mosaic trisomy 13 through 13/13 translocation and monosomy 13 with a small ring. [electronic resource] by Jalal, S M Martin, J A Benjamin, T R Kukolich, M K Townsend-Parcham, J K Producer: 19910328 In: Annales de genetique vol. 33 Availability: No items available. Save to lists Add to cart (remove)
	18.	A second autosomal split hand/split foot locus maps to chromosome 10q24-q25. [electronic resource] by Nunes, M E Schutt, G Kapur, R P Luthardt, F Kukolich, M Byers, P Evans, J P Producer: 19960327 In: Human molecular genetics vol. 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	19.	De novo supernumerary ring chromosome 7: first report of a non-mosaic patient and review of the literature. [electronic resource] by Velagaleti, G V N Jalal, S M Kukolich, M K Lockhart, L H Tonk, V S Producer: 20021212 In: Clinical genetics vol. 61 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	20.	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)

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Your search returned 28 results.