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Publications by Michelle Wyatt
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
Frontiers in Pediatrics
Child Health
Pediatrics
Perinatology
Chiari Malformation Associated With Craniosynostosis
Neurosurgical Focus
Medicine
Surgery
Neurology
PERK Interacts With FLNA to Regulate ER-PM Contact Sites
Oncotarget
Oncology
Nonsyndromic Craniosynostosis
Seminars in Plastic Surgery
Surgery
Association of Pathogenic Mutations in TULP1 With Retinitis Pigmentosa in Consanguineous Pakistani Families
Archives of Ophthalmology
Craniosynostosis, Philadelphia Type
Craniosynostosis-Syndactylism
American Journal of Roentgenology
Medicine
Nuclear Medicine
Radiology
Imaging
SRSF2 Mutations in Primary Myelofibrosis: Significant Clustering With IDH Mutations and Independent Association With Inferior Overall and Leukemia-Free Survival
Blood
Biochemistry
Immunology
Cell Biology
Hematology
IGF1R Variants Associated With Isolated Single Suture Craniosynostosis
American Journal of Medical Genetics, Part A
Genetics
