Genetic analysis of hereditary gingival fibromatosis using whole exome sequencing and bioinformatics.

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Genetic analysis of hereditary gingival fibromatosis using whole exome sequencing and bioinformatics.

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2016 nî lūn-bûn

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2016年の論文

@ja

2016年論文

@yue

2016年論文

@zh-hant

2016年論文

@zh-hk

2016年論文

@zh-mo

2016年論文

@zh-tw

2016年论文

@wuu

2016年论文

@zh

2016年论文

@zh-cn

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Genetic analysis of hereditary ...... sequencing and bioinformatics.

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Genetic analysis of hereditary ...... sequencing and bioinformatics.

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Genetic analysis of hereditary ...... sequencing and bioinformatics.

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P1476

Genetic analysis of hereditary ...... sequencing and bioinformatics

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P2093

D-H Han

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J Hwang

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S Kang

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S Kim

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S-O Kim

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Y-L Kim

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P2860

A mutation in the SOS1 gene causes hereditary gingival fibromatosis type 1

The basics of epithelial-mesenchymal transition

Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources

SH3 interactome conserves general function over specific form.

Homozygous frameshift mutation in TMCO1 causes a syndrome with craniofacial dysmorphism, skeletal anomalies, and mental retardation.

Refinement of the GINGF3 locus for hereditary gingival fibromatosis.

Homozygosity for a new mutation (Ile119-->Met) in the insulin receptor gene in five sibs with familial insulin resistance

Epithelial to mesenchymal transition in gingival overgrowth.

Evidence of genetic heterogeneity for hereditary gingival fibromatosis.

Genetic linkage of hereditary gingival fibromatosis to chromosome 2p21.

P304

102-109

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P31

scholarly article

P356

10.1111/ODI.12583

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P433

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P478

http://www.w3.org/2001/XMLSchema#string

P50

Jae-Hoon Lee

P577

2016-10-10T00:00:00Z

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P698

27614106

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P921

bioinformatics