Extending the phenotype of recurrent rearrangements of 16p11.2: Deletions in mentally retarded patients without autism and in normal individuals-Reference-Cited by-同舟云学术

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

Published:2009-03 Issue:2-3 Volume:52 Page:77-87
ISSN:1769-7212
Container-title:European Journal of Medical Genetics
language:en
Short-container-title:European Journal of Medical Genetics

Author:

Bijlsma E.K.,Gijsbers A.C.J.,Schuurs-Hoeijmakers J.H.M.,van Haeringen A.,Fransen van de Putte D.E.,Anderlid B.-M.,Lundin J.,Lapunzina P.,Pérez Jurado L.A.,Delle Chiaie B.,Loeys B.,Menten B.,Oostra A.,Verhelst H.,Amor D.J.,Bruno D.L.,van Essen A.J.,Hordijk R.,Sikkema-Raddatz B.,Verbruggen K.T.,Jongmans M.C.J.,Pfundt R.,Reeser H.M.,Breuning M.H.,Ruivenkamp C.A.L.

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics,General Medicine

Reference23 articles.

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