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	1.	Design of large-insert jumping libraries for structural variant detection using Illumina sequencing. [electronic resource] by Hanscom, C Talkowski, M Producer: 20160627 In: Current protocols in human genetics vol. 80 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Prenatal diagnosis of chromothripsis, with nine breaks characterized by karyotyping, FISH, microarray and whole-genome sequencing. [electronic resource] by Macera, M J Sobrino, A Levy, B Jobanputra, V Aggarwal, V Mills, A Esteves, C Hanscom, C Pereira, S Pillalamarri, V Ordulu, Z Morton, C C Talkowski, M Warburton, D Producer: 20151130 In: Prenatal diagnosis vol. 35 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Disruption of MBD5 contributes to a spectrum of psychopathology and neurodevelopmental abnormalities. [electronic resource] by Hodge, J C Mitchell, E Pillalamarri, V Toler, T L Bartel, F Kearney, H M Zou, Y S Tan, W H Hanscom, C Kirmani, S Hanson, R R Skinner, S A Rogers, R C Everman, D B Boyd, E Tapp, C Mullegama, S V Keelean-Fuller, D Powell, C M Elsea, S H Morton, C C Gusella, J F DuPont, B Chaubey, A Lin, A E Talkowski, M E Producer: 20141027 In: Molecular psychiatry vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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