BioMed Research International

Selected E2F2 Polymorphisms in Oral and Oropharyngeal Squamous Cell Carcinoma

TCF7L1 Genetic Variants Are Associated with the Susceptibility to Cervical Cancer in a Chinese Population

The Association between Five Genetic Variants in MicroRNAs (rs2910164, rs11614913, rs3746444, rs11134527, and rs531564) and Cervical Cancer Risk: A Meta-Analysis

Variant Analysis of Alkaptonuria Families with Significant Founder Effect in Jordan

A Novel COMP Mutated Allele Identified in a Chinese Family with Pseudoachondroplasia

Missense Variant of Endoplasmic Reticulum Region of WFS1 Gene Causes Autosomal Dominant Hearing Loss without Syndromic Phenotype

The Polymorphism Analyses of Short Tandem Repeats as a Basis for Understanding the Genetic Characteristics of the Guanzhong Han Population

Assessment on the Current State of On-Farm Diversity and Genetic Erosion in Barley (Hordeum vulgare L.) Landraces from Bale Highlands, Southeast Ethiopia

Identification of a Novel Homozygous Missense (c.443A>T:p.N148I) Mutation in BBS2 in a Kashmiri Family with Bardet-Biedl Syndrome

Retracted: Correlation of CCNA1 Promoter Methylation with Malignant Tumors: A Meta-Analysis Introduction

Association of BTLA Polymorphisms with Susceptibility to Non-Small-Cell Lung Cancer in the Chinese Population

Human ABO Blood Groups and Their Associations with Different Diseases

Associations between Inflammatory Cytokine Gene Polymorphisms and Susceptibilities to Intracranial Aneurysm in Chinese Population

MITF p.Arg217Thr Variant Identified in a Han Chinese Family with Tietz/Waardenburg Syndrome

Comprehensive Analysis of the Profiles of Differentially Expressed mRNAs, lncRNAs, and circRNAs in Phosgene-Induced Acute Lung Injury

BioMed Research International

Table of Contents

Table of Contents

Selected E2F2 Polymorphisms in Oral and Oropharyngeal Squamous Cell Carcinoma

TCF7L1 Genetic Variants Are Associated with the Susceptibility to Cervical Cancer in a Chinese Population

The Association between Five Genetic Variants in MicroRNAs (rs2910164, rs11614913, rs3746444, rs11134527, and rs531564) and Cervical Cancer Risk: A Meta-Analysis

Variant Analysis of Alkaptonuria Families with Significant Founder Effect in Jordan

A Novel COMP Mutated Allele Identified in a Chinese Family with Pseudoachondroplasia

Missense Variant of Endoplasmic Reticulum Region of WFS1 Gene Causes Autosomal Dominant Hearing Loss without Syndromic Phenotype

The Polymorphism Analyses of Short Tandem Repeats as a Basis for Understanding the Genetic Characteristics of the Guanzhong Han Population

Assessment on the Current State of On-Farm Diversity and Genetic Erosion in Barley (Hordeum vulgare L.) Landraces from Bale Highlands, Southeast Ethiopia

Identification of a Novel Homozygous Missense (c.443A>T:p.N148I) Mutation in BBS2 in a Kashmiri Family with Bardet-Biedl Syndrome

Retracted: Correlation of CCNA1 Promoter Methylation with Malignant Tumors: A Meta-Analysis Introduction

Association of BTLA Polymorphisms with Susceptibility to Non-Small-Cell Lung Cancer in the Chinese Population

Human ABO Blood Groups and Their Associations with Different Diseases

Associations between Inflammatory Cytokine Gene Polymorphisms and Susceptibilities to Intracranial Aneurysm in Chinese Population

MITF p.Arg217Thr Variant Identified in a Han Chinese Family with Tietz/Waardenburg Syndrome

Comprehensive Analysis of the Profiles of Differentially Expressed mRNAs, lncRNAs, and circRNAs in Phosgene-Induced Acute Lung Injury