Zheng ZJ - Search Results

1

Two novel isovaleryl-CoA dehydrogenase gene mutations in a Chinese infant.

Bei F, Sun JH, Yu YG, Jia J, Zheng ZJ, Fu QH, Cai W. Bei F, et al. Among authors: zheng zj. Gene. 2013 Jul 25;524(2):396-400. doi: 10.1016/j.gene.2013.03.139. Epub 2013 Apr 12. Gene. 2013. PMID: 23587913

2

Identification of LDLR mutations in two Chinese pedigrees with familial hypercholesterolemia.

Yao RE, Wang J, Geng J, Zheng Z, Yu T, Yu Y, Fu Q. Yao RE, et al. J Pediatr Endocrinol Metab. 2012;25(7-8):769-73. doi: 10.1515/jpem-2012-0024. J Pediatr Endocrinol Metab. 2012. PMID: 23155708

3

A unique combination of 17pter trisomy and 21qter monosomy in a boy with developmental delay, severe intellectual disability, growth retardation and dysmorphisms.

Zheng Z, Yao RE, Geng J, Jin X, Shen Y, Ying D, Fu Q, Yu Y. Zheng Z, et al. Gene. 2013 Mar 10;516(2):301-6. doi: 10.1016/j.gene.2012.12.090. Epub 2013 Jan 4. Gene. 2013. PMID: 23296059

4

Molecular defects identified by whole exome sequencing in a child with Fanconi anemia.

Zheng Z, Geng J, Yao RE, Li C, Ying D, Shen Y, Ying L, Yu Y, Fu Q. Zheng Z, et al. Gene. 2013 Nov 10;530(2):295-300. doi: 10.1016/j.gene.2013.08.031. Epub 2013 Aug 22. Gene. 2013. PMID: 23973728

5

A novel missense mutation of TNNI2 in a Chinese family cause distal arthrogryposis type 1.

Wang B, Zheng Z, Wang Z, Zhang X, Yang H, Cai H, Fu Q. Wang B, et al. Am J Med Genet A. 2016 Jan;170A(1):135-41. doi: 10.1002/ajmg.a.37391. Epub 2015 Sep 16. Am J Med Genet A. 2016. PMID: 26374086

6

Screening for coding variants in FTO and SH2B1 genes in Chinese patients with obesity.

Zheng Z, Hong L, Huang X, Yang P, Li J, Ding Y, Yao RE, Geng J, Shen Y, Shen Y, Fu Q, Yu Y. Zheng Z, et al. PLoS One. 2013 Jun 25;8(6):e67039. doi: 10.1371/journal.pone.0067039. Print 2013. PLoS One. 2013. PMID: 23825611 Free PMC article.

7

Three novel missense mutations in the filamin B gene are associated with isolated congenital talipes equinovarus.

Yang H, Zheng Z, Cai H, Li H, Ye X, Zhang X, Wang Z, Fu Q. Yang H, et al. Hum Genet. 2016 Oct;135(10):1181-9. doi: 10.1007/s00439-016-1701-7. Epub 2016 Jul 9. Hum Genet. 2016. PMID: 27395407

8

A novel GJA1 mutation identified by whole exome sequencing in a Chinese family with autosomal dominant syndactyly.

You G, Cai H, Jiang L, Zheng Z, Wang B, Fu Q, Wang J. You G, et al. Clin Chim Acta. 2016 Aug 1;459:73-78. doi: 10.1016/j.cca.2016.05.024. Epub 2016 May 27. Clin Chim Acta. 2016. PMID: 27241686 No abstract available.

9

Rare Copy Number Variations Might Not be Involved in the Molecular Pathogenesis of PA-IVS in an Unselected Chinese Cohort.

He X, Zhang X, Jing H, Zhang X, Gao M, Chen H, Geng J, Zheng Z, Fu Q, Zhu Z, Zheng J. He X, et al. Pediatr Cardiol. 2019 Apr;40(4):762-767. doi: 10.1007/s00246-019-02062-x. Epub 2019 Mar 13. Pediatr Cardiol. 2019. PMID: 30868185

10

Toll-like receptor 6 V327M polymorphism is associated with an increased risk of Klebsiella pneumoniae infection.

Yang H, Zhang X, Geng J, Zheng Z, Fu Q. Yang H, et al. Pediatr Infect Dis J. 2014 Nov;33(11):e310-5. doi: 10.1097/INF.0000000000000395. Pediatr Infect Dis J. 2014. PMID: 24797996

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

393 results

Search Page

Filters