European Journal of Human Genetics - Figure 1 for article: A further mutation of the FGFR2 tyrosine kinase domain in mild Crouzon syndrome

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A further mutation of the FGFR2 tyrosine kinase domain in mild Crouzon syndrome

Thomy J L de Ravel, Indira B Taylor, Alex J T Van Oostveldt, Jean-Pierre Fryns and Andrew O M Wilkie

Figure 1.

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Facial appearance of family members heterozygous for the FGFR2 mutation Lys526Glu. (a) Proband aged 7 years (left) and 28 years (centre and right, postoperative after Le Fort I osteotomy). (b) The proband's father aged 53 years. (c) The proband's sister aged 2 years (centre) and 23 years (right).

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FIGURE 1

A further mutation of the FGFR2 tyrosine kinase domain in mild Crouzon syndrome

Figure 1.