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Browsing by Author Sticht, H.

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Full TextIssue DateTitleAuthor(s)
2012Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing studyRauch, A.; Wieczorek, D.; Graf, E.; Wieland, T.; Endele, S., et al
2008Further delineation of Pitt-Hopkins syndrome: phenotypic and genotypic description of 16 novel patients.Zweier, C.; Sticht, H.; Bijlsma, E.K.; Clayton-Smith, J.; Boonen, S., et al
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