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	1.	Factor VII and factor X deficiency in a child with a chromosome 13q duplication and deletion. [electronic resource] by Hutchins, K Rajpurkar, M Stockton, D W Callaghan, M U Producer: 20210924 In: Haemophilia : the official journal of the World Federation of Hemophilia vol. 27 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Methylmalonic acidemia presenting as persistent pulmonary hypertension of the newborn. [electronic resource] by Agarwal, R Feldman, G L Poulik, J Stockton, D W Sood, B G Producer: 20150629 In: Journal of neonatal-perinatal medicine vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Mutation of PAX9 is associated with oligodontia. [electronic resource] by Stockton, D W Das, P Goldenberg, M D'Souza, R N Patel, P I Producer: 20000210 In: Nature genetics vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Characterization of the human beta4 nAChR gene and polymorphisms in CHRNA3 and CHRNB4. [electronic resource] by Lev-Lehman, E Bercovich, D Xu, W Stockton, D W Beaudet, A L Producer: 20011205 In: Journal of human genetics vol. 46 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Clinical, radiographic, and genetic evaluation of a novel form of autosomal-dominant oligodontia. [electronic resource] by Goldenberg, M Das, P Messersmith, M Stockton, D W Patel, P I D'Souza, R N Producer: 20010906 In: Journal of dental research vol. 79 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Delayed diagnosis of Friedreich's ataxia due to coexisting recessive deaf/blind syndrome. [electronic resource] by de Silva, R N Stockton, D W Keats, B Justice, C M Richards, C S Ashizawa, T Producer: 19980709 In: Neurology vol. 50 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Terminal osseous dysplasia with pigmentary defects maps to human chromosome Xq27.3-xqter. [electronic resource] by Zhang, W Amir, R Stockton, D W Van Den Veyver, I B Bacino, C A Zoghbi, H Y Producer: 20000531 In: American journal of human genetics vol. 66 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Severe clinical phenotype due to an interstitial deletion of the short arm of chromosome 1: a brief review. [electronic resource] by Stockton, D W Ross, H L Bacino, C A Altman, C A Shaffer, L G Lupski, J R Producer: 19970903 In: American journal of medical genetics vol. 71 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Terminal osseous dysplasia and pigmentary defects: clinical characterization of a novel male lethal X-linked syndrome. [electronic resource] by Bacino, C A Stockton, D W Sierra, R A Heilstedt, H A Lewandowski, R Van den Veyver, I B Producer: 20001019 In: American journal of medical genetics vol. 94 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	A novel locus for Leber congenital amaurosis on chromosome 14q24. [electronic resource] by Stockton, D W Lewis, R A Abboud, E B Al-Rajhi, A Jabak, M Anderson, K L Lupski, J R Producer: 19981119 In: Human genetics vol. 103 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Delineation of the critical interval of Bardet-Biedl syndrome 1 (BBS1) to a small region of 11q13, through linkage and haplotype analysis of 91 pedigrees. [electronic resource] by Katsanis, N Lewis, R A Stockton, D W Mai, P M Baird, L Beales, P L Leppert, M Lupski, J R Producer: 20000127 In: American journal of human genetics vol. 65 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Hereditary neuropathy with liability to pressure palsies is not a major cause of idiopathic carpal tunnel syndrome. [electronic resource] by Stockton, D W Meade, R A Netscher, D T Epstein, M J Shenaq, S M Shaffer, L G Lupski, J R Producer: 20011101 In: Archives of neurology vol. 58 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Multiple CYP1B1 mutations and incomplete penetrance in an inbred population segregating primary congenital glaucoma suggest frequent de novo events and a dominant modifier locus. [electronic resource] by Bejjani, B A Stockton, D W Lewis, R A Tomey, K F Dueker, D K Jabak, M Astle, W F Lupski, J R Producer: 20000504 In: Human molecular genetics vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent calcium channel. [electronic resource] by Zhuchenko, O Bailey, J Bonnen, P Ashizawa, T Stockton, D W Amos, C Dobyns, W B Subramony, S H Zoghbi, H Y Lee, C C Producer: 19970128 In: Nature genetics vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)