Pages that link to "Q55057321"
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The following pages link to Boston type craniosynostosis: report of a second mutation in MSX2. (Q55057321):
Displaying 12 items.
- Osterix/Sp7 limits cranial bone initiation sites and is required for formation of sutures (Q33792803) (← links)
- Neural crest cell signaling pathways critical to cranial bone development and pathology (Q33813000) (← links)
- Closing the Gap: Genetic and Genomic Continuum from Syndromic to Nonsyndromic Craniosynostoses. (Q35809894) (← links)
- Frontonasal Dysplasia: Towards an Understanding of Molecular and Developmental Aetiology. (Q37460161) (← links)
- Diagnostic value of exome and whole genome sequencing in craniosynostosis (Q37720856) (← links)
- CGtag: complete genomics toolkit and annotation in a cloud-based Galaxy (Q38400823) (← links)
- De novo mutations in inhibitors of Wnt, BMP, and Ras/ERK signaling pathways in non-syndromic midline craniosynostosis. (Q41614223) (← links)
- Genetic advances in craniosynostosis. (Q52795305) (← links)
- RETRACTED ARTICLE: Fetal methotrexate syndrome and Antley-Bixler syndrome should not be confused (Q61854983) (← links)
- Inherited Eye Diseases with Retinal Manifestations through the Eyes of Homeobox Genes (Q89944661) (← links)
- Current Approaches in the Development of Molecular and Pharmacological Therapies in Craniosynostosis Utilizing Animal Models (Q93043741) (← links)
- Rapid Low-Cost Microarray-Based Genotyping for Genetic Screening in Primary Immunodeficiency (Q94561533) (← links)