Extended clinical features associated with novel Glis3 mutation: a case report.

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Congenital hypothyroidism: insights into pathogenesis and treatment.GLIS1-3: emerging roles in reprogramming, stem and progenitor cell differentiation and maintenance.

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P2860

Extended clinical features associated with novel Glis3 mutation: a case report.

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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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name

Extended clinical features associated with novel Glis3 mutation: a case report.

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Extended clinical features associated with novel Glis3 mutation: a case report.

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Extended clinical features associated with novel Glis3 mutation: a case report.

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Extended clinical features associated with novel Glis3 mutation: a case report.

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Extended clinical features associated with novel Glis3 mutation: a case report.

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Extended clinical features associated with novel Glis3 mutation: a case report.

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Extended clinical features associated with novel Glis3 mutation: a case report

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A Aljasser

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A Altawil

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A B Alsaedi

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K A Alghamdi

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P2860

Characterization of Glis2, a novel gene encoding a Gli-related, Krüppel-like transcription factor with transactivation and repressor functions. Roles in kidney development and neurogenesis

Identification of NKL, a novel Gli-Kruppel zinc-finger protein that promotes neuronal differentiation

GLIS3, a novel member of the GLIS subfamily of Krüppel-like zinc finger proteins with repressor and activation functions

Identification of Glis1, a novel Gli-related, Kruppel-like zinc finger protein containing transactivation and repressor functions

Meta-analysis of genome-wide association studies identifies eight new loci for type 2 diabetes in east Asians.

Population-based birth defects data in the United States, 2008 to 2012: Presentation of state-specific data and descriptive brief on variability of prevalence.

TRANSCRIPTION FACTOR GLI-SIMILAR 3 (GLIS3): IMPLICATIONS FOR THE DEVELOPMENT OF CONGENITAL HYPOTHYROIDISM.

Hypospadias trends in two US surveillance systems.

Leptin may play a role in bone microstructural alterations in obese children.

Expanding the Clinical Spectrum Associated With GLIS3 Mutations.

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scholarly article

case report

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10.1186/S12902-017-0160-Z

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Naglaa Mohamed Kamal

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2017-03-02T00:00:00Z

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Extended clinical features associated with novel Glis3 mutation: a case report.

about

P2860

P2860

Extended clinical features associated with novel Glis3 mutation: a case report.

description

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type

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P1433

P1476

P2093

P2860

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