Longfei Cheng

发表

On the Origin of Tibetans and Their Genetic Basis in Adapting High-Altitude Environments

Jing Wang, Xu Ma, Jun Yu, 2011, PloS one.

The HHEX gene is not related to congenital heart disease in 296 Chinese patients

Binbin Wang, Longfei Cheng, Jing Wang, 2013, World Journal of Pediatrics.

Novel mutations of NODAL gene in Chinese patients with congenital heart disease.

Binbin Wang, Longfei Cheng, Jing Wang, 2012, Genetic testing and molecular biomarkers.

Identifying novel mutations of NKX2-5 congenital heart disease patients of Chinese minority groups.

Binbin Wang, Longfei Cheng, Jing Wang, 2011, International journal of cardiology.

Mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) in Chinese patients with congenital bilateral absence of vas deferens.

Xinyu Zhang, Binbin Wang, Longfei Cheng, 2012, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Functional Analysis of Two Novel Mutations in TWIST1 Protein Motifs Found in Ventricular Septal Defect Patients

Binbin Wang, Longfei Cheng, Jing Wang, 2015, Pediatric Cardiology.

Variations of the COL1A1 gene promoter and the relation to developmental dysplasia of the hip.

W. Tian, Binbin Wang, Longfei Cheng, 2013, Genetic testing and molecular biomarkers.

Two single nucleotide polymorphisms in the GDF5 gene are associated with development dysplasia of the hip in Chinese female population

Binbin Wang, Longfei Cheng, Jing Wang, 2013, Science China Life Sciences.

Association analysis between HOXD9 genes and the development of developmental dysplasia of the hip in Chinese female Han population

W. Tian, Binbin Wang, Longfei Cheng, 2012, BMC Musculoskeletal Disorders.

Two single-nucleotide polymorphisms in the DKK1 gene are associated with developmental dysplasia of the hip in the Chinese Han female population.

W. Tian, Longfei Cheng, Jing Wang, 2014, Genetic testing and molecular biomarkers.

A novel mutation of HOXA11 in a patient with septate uterus

Binbin Wang, Longfei Cheng, Jing Wang, 2017, Orphanet Journal of Rare Diseases.

A novel mutation of HOXA10 in a Chinese woman with a Mullerian duct anomaly.

Binbin Wang, Longfei Cheng, Jing Wang, 2011, Human reproduction.

Reproductive genetics A novel mutation of HOXA 10 in a Chinese woman with a Müllerian duct anomaly

Binbin Wang, Longfei Cheng, Jing Wang, 2011 .

Homeobox C9 is not potentially related to congenital heart disease in Chinese patients.

Binbin Wang, Longfei Cheng, Jing Wang, 2012, Genetic testing and molecular biomarkers.

Genetic association between BDNF gene polymorphisms and phobic disorders: a case-control study among mainland Han Chinese.

Binbin Wang, Longfei Cheng, Jing Wang, 2011, Journal of affective disorders.

Two single nucleotide polymorphisms in the GDF5 gene are associated with development dysplasia of the hip in Chinese female population

Binbin Wang, Longfei Cheng, Jing Wang, 2013, Science China Life Sciences.

Invasion of trophoblast cell lines is inhibited by miR-93 via MMP-2.

Longfei Cheng, Xiaoqiong Li, Q. Pan, 2017, Placenta.

HOXA1 Gene Is Not Potentially Related to Ventricular Septal Defect in Chinese Children

Binbin Wang, Longfei Cheng, Jing Wang, 2013, Pediatric Cardiology.

Polymorphisms in the Presumptive Promoter Region of the SLC2A9 Gene Are Associated with Gout in a Chinese Male Population

Dongmei Meng, Shiguo Liu, Binbin Wang, 2012, PloS one.

A novel non-synonymous mutation in the homeodomain of HOXD13 causes synpolydactyly in a Chinese family.

Xueya Zhou, Binbin Wang, Longfei Cheng, 2012, Clinica chimica acta; international journal of clinical chemistry.