No abstract available
MeSH terms
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Child
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Craniofacial Dysostosis / diagnosis
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Craniofacial Dysostosis / genetics*
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Developmental Disabilities / genetics
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Facies
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Female
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Heart Septal Defects, Ventricular / diagnosis
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Heart Septal Defects, Ventricular / genetics*
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Humans
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Intellectual Disability / genetics
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Middle Aged
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Mutation / genetics*
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Receptor, Fibroblast Growth Factor, Type 2 / genetics*
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Turkey
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Ultrasonography
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Ventricular Septum / diagnostic imaging
Substances
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FGFR2 protein, human
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Receptor, Fibroblast Growth Factor, Type 2