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- Bijlsma, EK (author)
Extending the phenotype of recurrent rearrangements of 16p11.2: deletions in mentally retarded patients without autism and in normal individuals
- Article/chapterEnglish2009
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- Elsevier BV,2009
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- LIBRIS-ID:oai:prod.swepub.kib.ki.se:118896263
- http://kipublications.ki.se/Default.aspx?queryparsed=id:118896263URI
- https://doi.org/10.1016/j.ejmg.2009.03.006DOI
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- Language:English
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- Gijsbers, ACJ (author)
- Schuurs-Hoeijmakers, JHM (author)
- van Haeringen, A (author)
- van de Putte, DEF (author)
- Anderlid, BMKarolinska Institutet (author)
- 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)
- Karolinska Institutet (creator_code:org_t)
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- In:European journal of medical genetics: Elsevier BV52:2-3, s. 77-871878-08491769-7212
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