Department of Paediatrics
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Browsing Department of Paediatrics by Subject "22q11.2 deletion syndrome"
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- ItemOpen AccessCover Image, Volume 173A, Number 4, April 2017(Wiley Periodicals, Inc., 2017-04) Kruszka, P.; Addissie, Y.A.; McGinn, D.E.; Porras, A.R.; Biggs, E.; Share, M.; Crowley, T.B.; Chung, B.H.Y.; Mok, G.T.K.; Muthukumarasamy, P.; Thong, M.; Sirisena, N.D.; Dissanayake, V.H.W.; Paththinige, C.S.; Prabodha, L.B.; Mishra, R.; Shotelersuk, V.; Ekure, E.N.; Sokunbi, O.J.; Kalu, N.; Ferreira, C.R.; Duncan, J.; Patil, S.J.; Jones, K.L.; Kaplan, J.D.; Abdul-Rahman, O.A.; Gil-da-Silva-Lopes, V.L.; Moresco, A.; Obregon, M.G.; Richieri-Costa, A.; Adeyemo, A.A.; Summar, M.; Zackai, E.H.; McDonald-McGinn, D.M.; Linguraru, M.G.; Muenke, M.The cover image, by Paul Kruszka et al., is based on the Original Article 22q11.2 deletion syndrome in diverse populations, DOI: 10.1002/ajmg.a.38199. Individual images are property of the National Human Genome Research Institute and are in the public domain.