Identical Mutation in SH3BP2 Gene Causes Clinical Phenotypes with Different Severity in Mother and Daughter - Case Report.
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Cherubism: best clinical practiceWhere genotype is not predictive of phenotype: towards an understanding of the molecular basis of reduced penetrance in human inherited disease.Novel nucleotide mutation leading to a recurrent amino acid alteration in SH3BP2 in a patient with cherubism.Clinicopathologic and Molecular Characteristics of Familial Cherubism with Associated Odontogenic Tumorous Proliferations.
P2860
Identical Mutation in SH3BP2 Gene Causes Clinical Phenotypes with Different Severity in Mother and Daughter - Case Report.
description
2010 nî lūn-bûn
@nan
2010 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Identical Mutation in SH3BP2 G ...... er and Daughter - Case Report.
@ast
Identical Mutation in SH3BP2 G ...... er and Daughter - Case Report.
@en
type
label
Identical Mutation in SH3BP2 G ...... er and Daughter - Case Report.
@ast
Identical Mutation in SH3BP2 G ...... er and Daughter - Case Report.
@en
prefLabel
Identical Mutation in SH3BP2 G ...... er and Daughter - Case Report.
@ast
Identical Mutation in SH3BP2 G ...... er and Daughter - Case Report.
@en
P2093
P2860
P356
P1476
Identical Mutation in SH3BP2 G ...... er and Daughter - Case Report.
@en
P2093
P2860
P356
10.1159/000314268
P50
P577
2010-06-09T00:00:00Z