An investigation of NFXL1, a gene implicated in a study of specific language impairment.

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An investigation of NFXL1, a gene implicated in a study of specific language impairment.

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2016 nî lūn-bûn

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2016年の論文

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2016年学术文章

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2016年学术文章

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2016年学术文章

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An investigation of NFXL1, a gene implicated in a study of specific language impairment.

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An investigation of NFXL1, a gene implicated in a study of specific language impairment.

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An investigation of NFXL1, a gene implicated in a study of specific language impairment.

@en

An investigation of NFXL1, a gene implicated in a study of specific language impairment.

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An investigation of NFXL1, a gene implicated in a study of specific language impairment.

@en

An investigation of NFXL1, a gene implicated in a study of specific language impairment.

@nl

P1476

An investigation of NFXL1, a gene implicated in a study of specific language impairment.

@en

P2093

Ron Nudel

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P2860

A novel cysteine-rich sequence-specific DNA-binding protein interacts with the conserved X-box motif of the human major histocompatibility complex class II genes via a repeated Cys-His domain and functions as a transcriptional repressor

What Causes Specific Language Impairment in Children?

Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method

GAPDH as a housekeeping gene: analysis of GAPDH mRNA expression in a panel of 72 human tissues

The Genotype-Tissue Expression (GTEx) project

Reorganizing the protein space at the Universal Protein Resource (UniProt)

An anatomically comprehensive atlas of the adult human brain transcriptome

Cloning and characterization of the CDZFP gene which encodes a putative zinc finger protein.

ChIP-Seq: technical considerations for obtaining high-quality data

Exome sequencing in an admixed isolated population indicates NFXL1 variants confer a risk for specific language impairment.

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s11689-016-9146-9

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scholarly article

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10.1186/S11689-016-9146-9

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2016-04-05T00:00:00Z

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1016822474

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27053962

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