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- Rees, E (author)
CNV analysis in a large schizophrenia sample implicates deletions at 16p12.1 and SLC1A1 and duplications at 1p36.33 and CGNL1
- Article/chapterEnglish2014
Publisher, publication year, extent ...
- 2013-10-26
- Oxford University Press (OUP),2014
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- LIBRIS-ID:oai:prod.swepub.kib.ki.se:128430467
- http://kipublications.ki.se/Default.aspx?queryparsed=id:128430467URI
- https://doi.org/10.1093/hmg/ddt540DOI
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- Language:English
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- SwePubSwePub
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- Walters, JTR (author)
- Chambert, KD (author)
- O'Dushlaine, C (author)
- Szatkiewicz, J (author)
- Richards, AL (author)
- Georgieva, L (author)
- Mahoney-Davies, G (author)
- Legge, SE (author)
- Moran, JL (author)
- Genovese, G (author)
- Levinson, D (author)
- Morris, DW (author)
- Cormican, P (author)
- Kendler, KS (author)
- O'Neill, FA (author)
- Riley, B (author)
- Gill, M (author)
- Corvin, A (author)
- Sklar, P (author)
- Hultman, CKarolinska Institutet (author)
- Pato, C (author)
- Pato, M (author)
- Sullivan, PFKarolinska Institutet (author)
- Gejman, PV (author)
- McCarroll, SA (author)
- O'Donovan, MC (author)
- Owen, MJ (author)
- Kirov, G (author)
- Karolinska Institutet (creator_code:org_t)
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- In:Human molecular genetics: Oxford University Press (OUP)23:6, s. 1669-16761460-20830964-6906
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- Hultman, C
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