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Multi-omics analysis reveals multiple mechanisms causing Prader-Willi like syndrome in a family with a X;15 translocation
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- Eisfeldt, J (author)
- Karolinska Institutet
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- Rezayee, F (author)
- Karolinska Institutet
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- Pettersson, M (author)
- Karolinska Institutet
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- 2022-07-23
- 2022
- English.
- In: Human mutation. - : Hindawi Limited. - 1098-1004 .- 1059-7794. ; 43:11, s. 1567-1575
- Journal article (peer-reviewed)
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- Eisfeldt, J
- Rezayee, F
- Pettersson, M
- Lagerstedt, K
- Malmgren, H
- Falk, A
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- Grigelioniene, G
- Lindstrand, A
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