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Publications by Karen M. Lyons

Bent Bone Dysplasia-Fgfr2 Type, a Distinct Skeletal Disorder, Has Deficient Canonical FGF Signaling

American Journal of Human Genetics
Genetics
2012English

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Bone Dysplasia, Lethal Holmgren Type

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A Case of Platyspondylic Lethal Skeletal Dysplasia Torrance Type

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The Bone Dysplasia Ontology: Integrating Genotype and Phenotype Information in the Skeletal Dysplasia Domain

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Distinct Fibroblast Growth Factor (FGF)/FGF Receptor Signaling Pairs Initiate Diverse Cellular Responses in the Oligodendrocyte Lineage

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Acrodysostosis - A Rare Skeletal Dysplasia

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Bone Robusticity in Two Distinct Skeletal Dysplasias Diverges From Established Patterns

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The Canonical Intrinsic Mitochondrial Death Pathway Has a Non-Apoptotic Role in Signaling Lens Cell Differentiation

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PI3K/AKT Signaling Determines a Dynamic Switch Between Distinct KSRP Functions Favoring Skeletal Myogenesis

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Presence of the Apert Canonical S252W FGFR2 Mutation in a Patient Without Severe Syndactyly.

Journal of Medical Genetics
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