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Browsing by Author Gardeitchik, T.
Showing results 4 to 6 of 6
| Full Text | Issue Date | Title | Author(s) | | 2011 | Metabolic cutis laxa syndromes | Mohamed, M.; Kouwenberg, D.; Gardeitchik, T., et al |
| 2011 | Nijmegen paediatric CDG rating scale: a novel tool to assess disease progression | Achouitar, S.; Mohamed, M.; Gardeitchik, T., et al |
| 2011 | Recognizable phenotype with common occurrence of microcephaly, psychomotor retardation, but no spontaneous bone fractures in autosomal recessive cutis laxa type IIB due to PYCR1 mutations | Kouwenberg, D.; Gardeitchik, T.; Wevers, R.A., et al |
Showing results 4 to 6 of 6
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