Further delineation of Malan syndrome
- Author(s):
- Priolo, M.; Schanze, D.; Tatton-Brown, K.; Mulder, P.A.; Tenorio, J.; Kooblall, K.; Acero, I.H.; Alkuraya, F.S.; Arias, P.; Bernardini, L.; Bijlsma, E.K.; Cole, T.; Coubes, C.; Dapia, I.; Davies, S.; Donato, N. di; Elcioglu, N.H.; Fahrner, J.A.; Foster, A.; Gonzalez, N.G.; Huber, I.; Iascone, M.; Kaiser, A.S.; Kamath, A.; Liebelt, J.; Lynch, S.A.; Maas, S.M.; Mammi, C.; Mathijssen, I.B.; McKee, S.; Menke, L.A.; Mirzaa, G.M.; Montgomery, T.; Neubauer, D.; Neumann, T.E.; Pintomalli, L.; Pisanti, M.A.; Plomp, A.S.; Price, S.; Salter, C.; Santos-Simarro, F.; Sarda, P.; Segovia, M.; Shaw-Smith, C.; Smithson, S.; Suri, M.; Valdez, R.M.; Haeringen, A. van; Hagen, J.M. van; Zollino, M.; Lapunzina, P.; Thakker, R.V.; Zenker, M.; Hennekam, R.C.
- Published
- 2018
- Publication type
- Article / Letter to editor
Malan syndromeMarshall-Smith syndromeNFIXphenotypephenotype-genotypeSotos syndromeWeaver syndrome
- Date issued
- 2018-09-30
- Language
- English
- Is part of
- Human Mutation (2018), Vol. 39, no. 9, p. 1226-1237
- hdl
- 1887/79628
- doi
- 10.1002/humu.23563
- URL
- https://onlinelibrary.wiley.com/doi/epdf/10.1002/humu.23563
