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

Bijlsma, EK (author)

Gijsbers, ACJ (author)

Schuurs-Hoeijmakers, JHM (author)

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van Haeringen, A (author)

van de Putte, DEF (author)

Anderlid, BM (author)

Karolinska Institutet

Lundin, J (author)

Lapunzina, P (author)

Jurado, LAP (author)

Delle Chiaie, B (author)

Loeys, B (author)

Menten, B (author)

Oostra, A (author)

Verhelst, H (author)

Amor, DJ (author)

Bruno, DL (author)

van Essen, AJ (author)

Hordijk, R (author)

Sikkema-Raddatz, B (author)

Verbruggen, KT (author)

Jongmans, MCJ (author)

Pfundt, R (author)

Reeser, HM (author)

Breuning, MH (author)

Ruivenkamp, CAL (author)

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 (creator_code:org_t)

Elsevier BV, 2009

2009

English.

In: European journal of medical genetics. - : Elsevier BV. - 1878-0849 .- 1769-7212. ; 52:2-3, s. 77-87

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• Journal article (peer-reviewed)