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Guidelines for reporting clinical features in cases with MECP2 mutations
- Kerr, AM (author)
- Nomura, Y (author)
- Armstrong, D (author)
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- Anvret, M (author)
- Belichenko, PV (author)
- Budden, S (author)
- Cass, H (author)
- Christodoulou, J (author)
- Clarke, A (author)
- Ellaway, C (author)
- d'Esposito, M (author)
- Francke, U (author)
- Hulten, M (author)
- Julu, P (author)
- Leonard, H (author)
- Naidu, S (author)
- Schanen, C (author)
- Webb, T (author)
- Engerstrom, IW (author)
- Yamashita, Y (author)
- Segawa, M (author)
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- Elsevier BV, 2001
- 2001
- English.
- In: Brain & development. - : Elsevier BV. - 0387-7604. ; 23:4, s. 208-211
- Journal article (peer-reviewed)
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- art (subject category)
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- Kerr, AM
- Nomura, Y
- Armstrong, D
- Anvret, M
- Belichenko, PV
- Budden, S
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- Cass, H
- Christodoulou, J
- Clarke, A
- Ellaway, C
- d'Esposito, M
- Francke, U
- Hulten, M
- Julu, P
- Leonard, H
- Naidu, S
- Schanen, C
- Webb, T
- Engerstrom, IW
- Yamashita, Y
- Segawa, M
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- Brain & developm ...
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- Karolinska Institutet
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