No abstract available
MeSH terms
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Abnormalities, Multiple / genetics*
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Craniosynostoses / genetics*
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Genotype
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Humans
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Phenotype
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Receptor Protein-Tyrosine Kinases / genetics*
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Receptor, Fibroblast Growth Factor, Type 2
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Receptors, Fibroblast Growth Factor / genetics*
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Syndrome
Substances
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Receptors, Fibroblast Growth Factor
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FGFR2 protein, human
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Receptor Protein-Tyrosine Kinases
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Receptor, Fibroblast Growth Factor, Type 2