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	21.	Maternal NLRP7 and C6orf221 variants are not a common risk factor for androgenetic moles, triploidy and recurrent miscarriage. [electronic resource] by Manokhina, I Hanna, C W Stephenson, M D McFadden, D E Robinson, W P Producer: 20140321 In: Molecular human reproduction vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	22.	Placental mesenchymal dysplasia associated with fetal overgrowth and mosaic deletion of the maternal copy of 11p15.5. [electronic resource] by Robinson, W P Slee, J Smith, N Murch, A Watson, S K Lam, W L McFadden, D E Producer: 20080116 In: American journal of medical genetics. Part A vol. 143A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	23.	Recurrent triploidy due to a failure to complete maternal meiosis II: whole-exome sequencing reveals candidate variants. [electronic resource] by Filges, I Manokhina, I Peñaherrera, M S McFadden, D E Louie, K Nosova, E Friedman, J M Robinson, W P Producer: 20151218 In: Molecular human reproduction vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	24.	The utility of quantitative methylation assays at imprinted genes for the diagnosis of fetal and placental disorders. [electronic resource] by Bourque, D K Peñaherrera, M S Yuen, R K C Van Allen, M I McFadden, D E Robinson, W P Producer: 20110308 In: Clinical genetics vol. 79 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	25.	Prenatal and postnatal inflammation in relation to cortisol levels in preterm infants at 18 months corrected age. [electronic resource] by Gover, A Chau, V Miller, S P Brant, R McFadden, D E Poskitt, K J Synnes, A Weinberg, J Grunau, R E Producer: 20140311 In: Journal of perinatology : official journal of the California Perinatal Association vol. 33 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	26.	Precise localisation of 3p25 breakpoints in four patients with the 3p-syndrome. [electronic resource] by Drumheller, T McGillivray, B C Behrner, D MacLeod, P McFadden, D E Roberson, J Venditti, C Chorney, K Chorney, M Smith, D I Producer: 19970221 In: Journal of medical genetics vol. 33 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	27.	Androgenetic/biparental mosaicism causes placental mesenchymal dysplasia. [electronic resource] by Kaiser-Rogers, K A McFadden, D E Livasy, C A Dansereau, J Jiang, R Knops, J F Lefebvre, L Rao, K W Robinson, W P Producer: 20060811 In: Journal of medical genetics vol. 43 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	28.	Comparison of phenotype in uniparental disomy and deletion Prader-Willi syndrome: sex specific differences. [electronic resource] by Mitchell, J Schinzel, A Langlois, S Gillessen-Kaesbach, G Schuffenhauer, S Michaelis, R Abeliovich, D Lerer, I Christian, S Guitart, M McFadden, D E Robinson, W P Producer: 19970219 In: American journal of medical genetics vol. 65 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)