about
Orodental phenotype and genotype findings in all subtypes of hypophosphatasiaOtodental syndromeA Novel Mutation in the ROGDI Gene in a Patient with Kohlschütter-Tönz SyndromeNephrocalcinosis (enamel renal syndrome) caused by autosomal recessive FAM20A mutationsHomozygosity mapping and candidate prioritization identify mutations, missed by whole-exome sequencing, in SMOC2, causing major dental developmental defectsSNP genome scanning localizes oto-dental syndrome to chromosome 11q13 and microdeletions at this locus implicate FGF3 in dental and inner-ear disease and FADD in ocular colobomaPhenotypic and evolutionary implications of modulating the ERK-MAPK cascade using the dentition as a model
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description
hulumtuese
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Agnès Bloch-Zupan
@ast
Agnès Bloch-Zupan
@en
Agnès Bloch-Zupan
@es
Agnès Bloch-Zupan
@nl
Agnès Bloch-Zupan
@sl
type
label
Agnès Bloch-Zupan
@ast
Agnès Bloch-Zupan
@en
Agnès Bloch-Zupan
@es
Agnès Bloch-Zupan
@nl
Agnès Bloch-Zupan
@sl
prefLabel
Agnès Bloch-Zupan
@ast
Agnès Bloch-Zupan
@en
Agnès Bloch-Zupan
@es
Agnès Bloch-Zupan
@nl
Agnès Bloch-Zupan
@sl