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Publications by Caroline Rooryck
Foetal Onset of EIF2B Related Disorder in Two Siblings: Cerebellar Hypoplasia With Absent Bergmann Glia and Severe Hypomyelination
Acta neuropathologica communications
Forensic Medicine
Molecular Neuroscience
Pathology
Neurology
Cellular
Deletion in 2q35 Excluding the IHH Gene Leads to Fetal Severe Limb Anomalies and Suggests a Disruption of Chromatin Architecture
European Journal of Human Genetics
Genetics
Prenatal Retinoic Acid Exposure Reveals Candidate Genes for Craniofacial Disorders
Scientific Reports
Multidisciplinary
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