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Extending the phenotype of recurrent rearrangements of 16p11.2: Deletions in mentally retarded patients without autism and in normal individuals

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Title: Extending the phenotype of recurrent rearrangements of 16p11.2: Deletions in mentally retarded patients without autism and in normal individuals
Authors: Bijlsma, E.K.1 e.k.bijlsma@lumc.nl, Gijsbers, A.C.J.1, Schuurs-Hoeijmakers, J.H.M.1, van Haeringen, A.1, Fransen van de Putte, D.E.1, Anderlid, B.-M.2, Lundin, J.2, Lapunzina, P.3,4, Pérez Jurado, L.A.5,6, Delle Chiaie, B.7, Loeys, B.7, Menten, B.7, Oostra, A.7, Verhelst, H.8, Amor, D.J.9,10, Bruno, D.L.9,10, van Essen, A.J.11, Hordijk, R.11, Sikkema-Raddatz, B.11, Verbruggen, K.T.12
Source: European Journal of Medical Genetics. Mar2009, Vol. 52 Issue 2/3, p77-87. 11p.
Database: Academic Search Ultimate
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  Data: Extending the phenotype of recurrent rearrangements of 16p11.2: Deletions in mentally retarded patients without autism and in normal individuals
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