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

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

Book ID: 116433173
Publisher: Elsevier Science
Year: 2009
Tongue: English
Weight: 655 KB
Volume: 52
Category: Article
ISSN: 1769-7212
DOI: 10.1016/j.ejmg.2009.03.006

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