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Browsing by Author Gardeitchik, T.

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Full TextIssue DateTitleAuthor(s)
2011Recognizable phenotype with common occurrence of microcephaly, psychomotor retardation, but no spontaneous bone fractures in autosomal recessive cutis laxa type IIB due to PYCR1 mutationsKouwenberg, D.; Gardeitchik, T.; Wevers, R.A., et al
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