Hong Chen

发表

The tRNAMet 4435A>G mutation in the mitochondrial haplogroup G2a1 is responsible for maternally inherited hypertension in a Chinese pedigree

Yan Wang, J. Mo, M. Guan, 2011, European Journal of Human Genetics.

Lipoid congenital adrenal hyperplasia due to steroid acute regulatory protein (STAR) variants in Three Chinese patients

Hong Chen, Qianru Zhang, Ruimin Chen, 2020, The Journal of Steroid Biochemistry and Molecular Biology.

Identification of dysregulated microRNAs in lymphocytes from children with Down syndrome.

Yong Dai, Z. Tu, Yong Xu, 2013, Gene.

[Association of copy number of SMN1 and SMN2 with clinical phenotypes in children with spinal muscular atrophy].

Jie Zhang, Jing He, Hong Chen, 2019, Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics.

Analysis of deletional hereditary persistence of fetal hemoglobin/δβ‐thalassemia and δ‐globin gene mutations in Southerwestern China

Tonghua Yang, P. Li, Jie Zhang, 2019, Molecular genetics & genomic medicine.

Molecular epidemiology, pathogenicity, and structural analysis of haemoglobin variants in the Yunnan province population of Southwestern China

Peng Li, Jie Zhang, Hong Chen, 2019, Scientific Reports.

The Spectrum of α- And β-Thalassemia Mutations in Yunnan Province of Southwestern China

Jie Zhang, Jing He, Hong Chen, 2012, Hemoglobin.

[A study on gene mutation spectrums of α- and β-thalassemias in populations of Yunnan Province and the prenatal gene diagnosis].

Jie Zhang, Jing He, Hong Chen, 2012, Zhonghua fu chan ke za zhi.

Fanconi anemia pathway defects in inherited and sporadic cancers.

Hong Chen, Zhanhe Wu, Shuxia Zhang, 2014, Translational pediatrics.

Rare exonic deletions implicate the synaptic organizer Gephyrin (GPHN) in risk for autism, schizophrenia and seizures.

S. Scherer, G. Kirov, D. Merico, 2013, Human molecular genetics.

Hypertension-associated mitochondrial DNA 4401A>G mutation caused the aberrant processing of tRNAMet, all 8 tRNAs and ND6 mRNA in the light-strand transcript

Yuqi Liu, Meng Wang, M. Guan, 2019, Nucleic acids research.

Mitochondrial C4375T mutation might be a molecular risk factor in a maternal Chinese hypertensive family under haplotype C

Hong Chen, Jihui Ye, Guo-dong Chen, 2018, Clinical and experimental hypertension.

[Analysis of treatment efficacy for congenital hypothyroidism in some regions of Yunnan Province, China].

Z. Wang, Y. Li, Hong Chen, 2017, Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics.

[Study on key techniques and intervention in reducing birth defects].

Jing He, Hong Chen, Jin-man Zhang, 2011, Zhonghua fu chan ke za zhi.

The 12S rRNA A1555G mutation in the mitochondrial haplogroup D5a is responsible for maternally inherited hypertension and hearing loss in two Chinese pedigrees

Yan Wang, Bin Zheng, J. Mo, 2012, European Journal of Human Genetics.

Novel DOCK7 mutations in a Chinese patient with early infantile epileptic encephalopathy 23

Hong Chen, B. Bai, Jin-man Zhang, 2019, Chinese medical journal.

[Mutations in mitochondrial DNA associated with hypertension].

Yan Wang, M. Guan, L. Xue, 2011, Yi chuan = Hereditas.