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	1.	Deletion of 7q31.1 supports involvement of FOXP2 in language impairment: clinical report and review. [electronic resource] by Lennon, P A Cooper, M L Peiffer, D A Gunderson, K L Patel, A Peters, Sarika Cheung, S W Bacino, C A Producer: 20070516 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)
	2.	Characterization of de novo microdeletions involving 17q11.2q12 identified through chromosomal comparative genomic hybridization. [electronic resource] by Brunetti-Pierri, N Grange, D K Ou, Z Peiffer, D A Peacock, S K G Cooper, M L Eng, P A Lalani, S R Chinault, A C Gunderson, K L Craigen, W J Cheung, S-W Producer: 20080104 In: Clinical genetics vol. 72 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Identification of critical regions for clinical features of distal 10q deletion syndrome. [electronic resource] by Yatsenko, S A Kruer, M C Bader, P I Corzo, D Schuette, J Keegan, C E Nowakowska, B Peacock, S Cai, W W Peiffer, D A Gunderson, K L Ou, Z Chinault, A C Cheung, S W Producer: 20091007 In: Clinical genetics vol. 76 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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