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Paper Details
Paper Title
Common genetic causes of holoprosencephaly are limited to a small set of evolutionarily conserved driver genes of midline development coordinated by TGF-β, hedgehog, and FGF signaling.
PubMed
Paper Journal Title
Hum Mutat
Paper Citation Count
21
Paper Publication Year
2018
Bio Mention
153 genes, FGF, HPE, TGF, driver genes, holoprosencephaly, novel genes
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Author Name
Affiliation
Seth I Berger
National Human Genome Research Institute, National Institutes of Health
James C Mullikin
National Human Genome Research Institute, National Institutes of Health
James C Mullikin
National Human Genome Research Institute, National Institutes of Health
Benjamin D Solomon
Inova Translational Medicine Institute, Virginia Commonwealth University School of Medicine
Benjamin D Solomon
Maximilian Muenke
National Human Genome Research Institute, National Institutes of Health
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