Q289P mutation in FGFR2 gene causes Saethre-Chotzen syndrome: some considerations about familial heterogeneity.
about
Mutational identification of fibroblast growth factor receptor 1 and fibroblast growth factor receptor 2 genes in craniosynostosis in Indian population.Exclusion of Class III malocclusion candidate loci in Brazilian families.Saethre-Chotzen syndrome: a case report.Fibroblast Growth Factor Receptor 2 (FGFR2) Mutation Related Syndromic Craniosynostosis.
P2860
Q289P mutation in FGFR2 gene causes Saethre-Chotzen syndrome: some considerations about familial heterogeneity.
description
2006 nî lūn-bûn
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Q289P mutation in FGFR2 gene c ...... about familial heterogeneity.
@en
Q289P mutation in FGFR2 gene c ...... about familial heterogeneity.
@nl
type
label
Q289P mutation in FGFR2 gene c ...... about familial heterogeneity.
@en
Q289P mutation in FGFR2 gene c ...... about familial heterogeneity.
@nl
prefLabel
Q289P mutation in FGFR2 gene c ...... about familial heterogeneity.
@en
Q289P mutation in FGFR2 gene c ...... about familial heterogeneity.
@nl
P2093
P356
P1476
Q289P mutation in FGFR2 gene c ...... s about familial heterogeneity
@en
P2093
Erika Cristina Lopes Burrone de Freitas
Maricilda Palandi de Mello
Sandra Regina Dantas Nascimento
P2860
P304
P356
10.1597/04-155.1
P407
P577
2006-03-01T00:00:00Z