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V. C. Daire
V. C. Daire
Paris Descartes University
Internal medicine
Missense mutation
Tyrosine
Endocrinology
Gene
1
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6
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Crouzon syndrome and Bent bone dysplasia associated with mutations at the same Tyr‐381 residue in FGFR2 gene
2014
Clinical Genetics
Corinne Collet
Jean-Luc Alessandri
E. Arnaud
M. Balu
V. C. Daire
F. Di Rocco
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Citations (6)
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