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	Title	Author(s)	Issue Date	Views
	22q11.2 deletion syndrome in diverse populations Journal:American Journal of Medical Genetics Part A	Kruszka, P Addissie, YA McGinn, DE Porras, AR Biggs, E Share, M Crowley, TB Chung, BHY Mok, TKG MAK, CCY Muthukumarasamy, P Thong, MK Siriseria, ND Dissanayake, VHW Paththinige, CS Prabodha, LBL Mishra, R Shotelersuk, V Ekure, EN Sokunbi, OJ Kalu, N Ferreira, CR Duncan, JM Patil, SJ Jones, KL Kaplan, JD Abdul-Rahman, OA Uwineza, A Mutesa, L Moresco, A Obregon, MG Richieri-Costa, A Gil-da-Silva-Lopes, VL Adeyemo, AA Summar, M Zackai, EH McDonald-McGinn, DM Linguraru, MG Muenke, M	2017	71
	Human chromosome 7: DNA sequence and biology Journal:Science	Scherer, SW Cheung, J MacDonald, JR Osborne, LR Nakabayashi, K Herbrick, JA Carson, AR ParkerKatiraee, L Skaug, J Khaja, R Zhang, J Hudek, AK Li, M Haddad, M Duggan, GE Fernandez, BA Kanematsu, E Gentles, S Christopoulos, CC Choufani, S Kwasnicka, D Zheng, XH Lai, Z Nusskern, D Zhang, Q Gu, Z Lu, F Zeesman, S Nowaczyk, MJ Teshima, I Chitayat, D Shuman, C Weksberg, R Zackai, EH Grebe, TA Cox, SR Kirkpatrick, SJ Rahman, N Friedman, JM Heng, HHQ Pelicci, PG LoCoco, F Belloni, E Shaffer, LG Pober, B Morton, CC Gusella, JF Bruns, GAP Korf, BR Quade, BJ Ligon, AH Ferguson, H Higgins, AW Leach, NT Herrick, SR Lemyre, E Farra, CG Kim, HG Summers, AM Gripp, KW Roberts, W Szatmari, P Winsor, EJT Grzeschik, KH Teebi, A Minassian, BA Kere, J Armengol, L Pujana, MA Estivill, X Wilson, MD Koop, BF Tosi, S Moore, GE Boright, AP Zlotorynski, E Kerem, B Kroisel, PM Petek, E Oscier, DG Mould, SJ Döhner, H Döhner, K Rommens, JM Vincent, JB Venter, JC Li, PW Mural, RJ Adams, MD Tsui, LC	2003	142
	Limb body wall complex, amniotic band sequence, or new syndrome caused by mutation in IQ Motif containing K (IQCK)? Journal:Molecular Genetics & Genomic Medicine	Kruszka, P Uwineza, A Mutesa, L Martinez, AF Abe, Y Zackai, EH Ganetzky, R Chung, BHY Stevenson, RE Adelstein, RS Ma, X Mullikin, JC Hong, SK Muenke, M	2015	40
	Recurrent de novo missense mutations in PP1CB cause a novel rasopathy closely resembling Noonan syndrome with loose anagen hair (Reviewer choice) Proceeding/Conference:Asian Society for Pediatric Research & Faculty of Medicine Ramathibodi Hospital Joint Meeting, ASPR 2016	Gripp, KW Aldinger, KA Bennett, J Baker, L Tusi, J Powell-Hamilton, N Stabley, D Sol-Church, K Timms, A Dobyns, WB de Man, A Larson, A Spruijt, L Koolen, D Stevens, SJC Stegmann, APA Nillesen, MW Norrhock, HV Belien, M Nellist, M Verheijen, F Wilems, PJ Chung, BHY Dubbs, H Bhoj, E Santani, A McDougall, C Zackai, EH Rinne, TK Wessels, MW	2016	49

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