A microdeletion in the GRHL2 Gene in two unrelated patients with congenital fibrosis of the extra ocular muscles.

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A microdeletion in the GRHL2 Gene in two unrelated patients with congenital fibrosis of the extra ocular muscles.

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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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A microdeletion in the GRHL2 G ...... s of the extra ocular muscles.

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A microdeletion in the GRHL2 G ...... s of the extra ocular muscles.

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Item

label

A microdeletion in the GRHL2 G ...... s of the extra ocular muscles.

@en

A microdeletion in the GRHL2 G ...... s of the extra ocular muscles.

@nl

prefLabel

A microdeletion in the GRHL2 G ...... s of the extra ocular muscles.

@en

A microdeletion in the GRHL2 G ...... s of the extra ocular muscles.

@nl

P1476

A microdeletion in the GRHL2 G ...... s of the extra ocular muscles.

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Altaf A Kondkar

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Arif O Khan

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Khaled K Abu-Amero

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P2860

Dual roles of the transcription factor grainyhead-like 2 (GRHL2) in breast cancer

Mutations in GRHL2 result in an autosomal-recessive ectodermal Dysplasia syndrome

Chromosomal duplication involving the forkhead transcription factor gene FOXC1 causes iris hypoplasia and glaucoma

The clinical spectrum of homozygous HOXA1 mutations

Mutation of a transcription factor, TFCP2L3, causes progressive autosomal dominant hearing loss, DFNA28

Mutations at the PAX6 locus are found in heterogeneous anterior segment malformations including Peters' anomaly

The transcription factor grainyhead-like 2 regulates the molecular composition of the epithelial apical junctional complex

Association between genetic variations in GRHL2 and noise-induced hearing loss in Chinese high intensity noise exposed workers: a case-control analysis.

Functional conservation between members of an ancient duplicated transcription factor family, LSF/Grainyhead.

Duane's syndrome.

P2888

s13104-017-2888-y

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scholarly article

case report

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10.1186/S13104-017-2888-Y

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2017-11-06T00:00:00Z

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1092562975

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29110737

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