Novel variant syndrome associated with congenital hepatic fibrosis.

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A Challenging Case of Hepatoblastoma Concomitant with Autosomal Recessive Polycystic Kidney Disease and Caroli Syndrome-Review of the Literature.

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Novel variant syndrome associated with congenital hepatic fibrosis.

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2015 nî lūn-bûn

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2015年の論文

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2015年論文

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2015年論文

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2015年論文

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2015年論文

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2015年论文

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name

Novel variant syndrome associated with congenital hepatic fibrosis.

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Novel variant syndrome associated with congenital hepatic fibrosis.

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Novel variant syndrome associated with congenital hepatic fibrosis.

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Novel variant syndrome associated with congenital hepatic fibrosis.

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Novel variant syndrome associated with congenital hepatic fibrosis.

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Novel variant syndrome associated with congenital hepatic fibrosis.

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Novel variant syndrome associated with congenital hepatic fibrosis.

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Cenk Sokmensuer

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Hande Taylan

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Kubilay Varlı

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Ozlem Yonem

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Yusuf Bayraktar

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Cohen syndrome is caused by mutations in a novel gene, COH1, encoding a transmembrane protein with a presumed role in vesicle-mediated sorting and intracellular protein transport

The Meckel-Gruber syndrome gene, MKS3, is mutated in Joubert syndrome

New criteria for improved diagnosis of Bardet-Biedl syndrome: results of a population survey

The Meckel syndrome: clinicopathological findings in 67 patients

Retinitis pigmentosa

Cerebello-oculo-renal syndromes including Arima, Senior-Löken and COACH syndromes: more than just variants of Joubert syndrome.

COACH syndrome associated with multifocal liver tumors.

A new syndrome with hypotonia, obesity, mental deficiency, and facial, oral, ocular, and limb anomalies.

Joubert syndrome: a review.

Is congenital hepatic fibrosis a pure liver disease?

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scholarly article

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10.12998/WJCC.V3.I10.904

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Ali Shorbagi

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2015-10-01T00:00:00Z

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283077394

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26488028

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birth defect

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4607810

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Novel variant syndrome associated with congenital hepatic fibrosis.

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P2860

P2860

Novel variant syndrome associated with congenital hepatic fibrosis.

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