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Issue Date
Title
Author(s)
1997
A unique point mutation in the fibroblast growth factor receptor 3 gene (FGFR3) defines a new craniosynostosis syndrome
Muenke, M.
;
Gripp, K.
;
McDonald-McGinn, D.
;
Gaudenz, K.
;
Whitaker, L.
;
Bartlett, S.
;
Markowitz, R.
;
Robin, N.
;
Nwokoro, N.
;
Mulvihill, J.
;
Losken, H.
;
Mulliken, J.
;
Guttmacher, A.
;
Wilroy, R.
;
Clarke, L.
;
Hollway, G.
;
Ades, L.
;
Haan, E.
;
Mulley, J.
;
Cohen, M.
;
et al.
Discover
Author
1
Ades, L.
1
Clarke, L.
1
Cohen, M.
1
et al.
1
Gaudenz, K.
1
Gripp, K.
1
Guttmacher, A.
1
Hollway, G.
1
Losken, H.
1
Markowitz, R.
.
next >
Subject
1
Chromosomes, Human, Pair 4
1
Craniosynostoses
1
Foot Deformities, Congenital
1
Humans
1
Male
1
Point Mutation
1
Protein-Tyrosine Kinases
1
Receptor, Fibroblast Growth Facto...
1
Receptors, Fibroblast Growth Factor
1
Syndrome
.
next >
Date issued
1
1997