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	1.	Choices of incidental findings of individuals undergoing genome wide sequencing, a single center's experience. [electronic resource] by Bishop, C L Strong, K A Dimmock, D P Producer: 20170613 In: Clinical genetics vol. 91 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	A novel FOXF1 mutation associated with alveolar capillary dysplasia and coexisting colobomas and hemihyperplasia. [electronic resource] by Geddes, G C Dimmock, D P Hehir, D A Helbling, D C Kirkpatrick, E Loomba, R Southern, J Waknitz, M Scharer, G Konduri, G G Producer: 20151026 In: Journal of perinatology : official journal of the California Perinatal Association vol. 35 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Clinical and molecular features of mitochondrial DNA depletion due to mutations in deoxyguanosine kinase. [electronic resource] by Dimmock, D P Zhang, Q Dionisi-Vici, C Carrozzo, R Shieh, J Tang, L-Y Truong, C Schmitt, E Sifry-Platt, M Lucioli, S Santorelli, F M Ficicioglu, C H Rodriguez, M Wierenga, K Enns, G M Longo, N Lipson, M H Vallance, H Craigen, W J Scaglia, F Wong, L-J Producer: 20080207 In: Human mutation vol. 29 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Guidelines for investigating causality of sequence variants in human disease. [electronic resource] by MacArthur, D G Manolio, T A Dimmock, D P Rehm, H L Shendure, J Abecasis, G R Adams, D R Altman, R B Antonarakis, S E Ashley, E A Barrett, J C Biesecker, L G Conrad, D F Cooper, G M Cox, N J Daly, M J Gerstein, M B Goldstein, D B Hirschhorn, J N Leal, S M Pennacchio, L A Stamatoyannopoulos, J A Sunyaev, S R Valle, D Voight, B F Winckler, W Gunter, C Producer: 20140813 In: Nature vol. 508 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)