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Publications by Nathalie Fennell
Association of Mutations in FLNA With Craniosynostosis
European Journal of Human Genetics
Genetics
Related publications
Phenotypic Overlap of Roberts and Baller-Gerold Syndromes in Two Patients With Craniosynostosis, Limb Reductions, and ESCO2 Mutations
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Neurosurgical Focus
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PERK Interacts With FLNA to Regulate ER-PM Contact Sites
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Association of Pathogenic Mutations in TULP1 With Retinitis Pigmentosa in Consanguineous Pakistani Families
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SRSF2 Mutations in Primary Myelofibrosis: Significant Clustering With IDH Mutations and Independent Association With Inferior Overall and Leukemia-Free Survival
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IGF1R Variants Associated With Isolated Single Suture Craniosynostosis
American Journal of Medical Genetics, Part A
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