Novel FAM83H mutations in patients with amelogenesis imperfecta.

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Novel FAM83H mutations in patients with amelogenesis imperfecta.

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年學術文章

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2017年學術文章

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2017年學術文章

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Novel FAM83H mutations in patients with amelogenesis imperfecta.

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Novel FAM83H mutations in patients with amelogenesis imperfecta.

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Novel FAM83H mutations in patients with amelogenesis imperfecta.

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P1476

Novel FAM83H mutations in patients with amelogenesis imperfecta.

@en

P2093

Qin Man

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

Wang Wenjun

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

Wang Xin

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

Zhao Yuming

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P2860

Whole-Exome sequencing identifies FAM20A mutations as a cause of amelogenesis imperfecta and gingival hyperplasia syndrome

Novel WDR72 mutation and cytoplasmic localization

A novel mechanism of keratin cytoskeleton organization through casein kinase Iα and FAM83H in colorectal cancer

STIM1 and SLC24A4 Are Critical for Enamel Maturation

ITGB6 loss-of-function mutations cause autosomal recessive amelogenesis imperfecta

Mutational spectrum of FAM83H: the C-terminal portion is required for tooth enamel calcification

FAM83H mutations in families with autosomal-dominant hypocalcified amelogenesis imperfecta

DLX3 mutation associated with autosomal dominant amelogenesis imperfecta with taurodontism

Target gene analyses of 39 amelogenesis imperfecta kindreds

Recessive Mutations in ACPT, Encoding Testicular Acid Phosphatase, Cause Hypoplastic Amelogenesis Imperfecta

P2888

s41598-017-05208-0

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6075

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scholarly article

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10.1038/S41598-017-05208-0

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P407

English

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P478

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

P577

2017-07-20T00:00:00Z

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28729668

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P932

5519741

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