Category:Pfeiffer syndrome
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acrocephalosyndactylia that has material basis in mutations in the FGFR1 and FGFR2 gene which results in premature fusion located in skull | |||||
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Media in category "Pfeiffer syndrome"
The following 13 files are in this category, out of 13 total.
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Chinese circus performer with craniosynostosis, 1927.jpg 1,200 × 1,704; 122 KB
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Davis Oxycephalus 3.jpg 741 × 969; 110 KB
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Davis Oxycephalus 4.jpg 595 × 960; 86 KB
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Fletcher Oxycephaly 17.jpg 694 × 755; 109 KB
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Fletcher Oxycephaly 18.jpg 749 × 1,060; 107 KB
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Fletcher Oxycephaly 19.jpg 751 × 1,056; 106 KB
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Fletcher Oxycephaly 20.jpg 1,303 × 1,099; 137 KB
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Girl aged 17 years with marked proptosis Wellcome L0062480.jpg 4,175 × 5,856; 6.89 MB
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Girl aged 17 years with marked proptosis Wellcome L0062481.jpg 3,974 × 5,267; 2.6 MB
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Lewin Acrocephaly 1.jpg 620 × 824; 88 KB
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Lewin Acrocephaly 2.jpg 628 × 812; 85 KB
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Weygandt 1.jpg 669 × 768; 90 KB