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Targeted copy number screening highlights an intragenic deletion of WDR63 as the likely cause of human occipital encephalocele and abnormal CNS development in zebrafish

Hofmeister, W (author)
Karolinska Institutet
Pettersson, M (author)
Karolinska Institutet
Kurtoglu, D (author)
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Armenio, M (author)
Eisfeldt, J (author)
Karolinska Institutet
Papadogiannakis, N (author)
Karolinska Institutet
Gustavsson, P (author)
Karolinska Institutet
Lindstrand, A (author)
Karolinska Institutet
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 (creator_code:org_t)
2018-01-11
2018
English.
In: Human mutation. - : Hindawi Limited. - 1098-1004 .- 1059-7794. ; 39:4, s. 495-505
  • Journal article (peer-reviewed)
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