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You searched for: Author/Creator Guilmin Crepon, Sophie

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1. Autosomal recessive primary microcephaly due to ASPM mutations: An update. Issue 3 (16th January 2018)

2. CDK5RAP2 primary microcephaly is associated with hypothalamic, retinal and cochlear developmental defects. Issue 6 (3rd February 2020)

3. Neurological outcome in WDR62 primary microcephaly. (25th September 2021)