Wang B - Search Results

1

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. Among authors: wang z. 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

2

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. Among authors: wang j, wang b. 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.

3

Exome sequencing identifies a novel nonsense mutation of HOXD13 in a Chinese family with synpolydactyly.

Wang B, Li N, Geng J, Wang Z, Fu Q, Wang J, Xu Y. Wang B, et al. Among authors: wang z, wang j. Congenit Anom (Kyoto). 2017 Jan;57(1):4-7. doi: 10.1111/cga.12173. Congenit Anom (Kyoto). 2017. PMID: 27254532

4

A Novel Missense Mutation of GATA4 in a Chinese Family with Congenital Heart Disease.

Zhang X, Wang J, Wang B, Chen S, Fu Q, Sun K. Zhang X, et al. Among authors: wang j, wang b. PLoS One. 2016 Jul 8;11(7):e0158904. doi: 10.1371/journal.pone.0158904. eCollection 2016. PLoS One. 2016. PMID: 27391137 Free PMC article.

5

Mutational screening of GLI3, SHH, preZRS, and ZRS in 102 Chinese children with nonsyndromic polydactyly.

Xiang Y, Jiang L, Wang B, Xu Y, Cai H, Fu Q. Xiang Y, et al. Among authors: wang b. Dev Dyn. 2017 May;246(5):392-402. doi: 10.1002/dvdy.24488. Epub 2017 Feb 27. Dev Dyn. 2017. PMID: 28127823 Free article.

6

Exome Sequencing Identified a Novel FBN2 Mutation in a Chinese Family with Congenital Contractural Arachnodactyly.

You G, Zu B, Wang B, Wang Z, Xu Y, Fu Q. You G, et al. Among authors: wang z, wang b. Int J Mol Sci. 2017 Apr 5;18(4):626. doi: 10.3390/ijms18040626. Int J Mol Sci. 2017. PMID: 28379158 Free PMC article.

7

Human fetal heart specific coexpression network involves congenital heart disease/defect candidate genes.

Wang B, You G, Fu Q. Wang B, et al. Sci Rep. 2017 Apr 24;7:46760. doi: 10.1038/srep46760. Sci Rep. 2017. PMID: 28436429 Free PMC article.

8

Accurate diagnosis of spinal muscular atrophy and 22q11.2 deletion syndrome using limited deoxynucleotide triphosphates and high-resolution melting.

Zhang X, Wang B, Zhang L, You G, Palais RA, Zhou L, Fu Q. Zhang X, et al. Among authors: wang b. BMC Genomics. 2018 Jun 20;19(1):485. doi: 10.1186/s12864-018-4833-4. BMC Genomics. 2018. PMID: 29925309 Free PMC article.

9

Sexual difference of small RNA expression in Tetralogy of Fallot.

Wang B, Shi G, Zhu Z, Chen H, Fu Q. Wang B, et al. Sci Rep. 2018 Aug 27;8(1):12847. doi: 10.1038/s41598-018-31243-6. Sci Rep. 2018. PMID: 30150777 Free PMC article.

10

15q11.2 deletion is enriched in patients with total anomalous pulmonary venous connection.

Li X, Shi G, Li Y, Zhang X, Xiang Y, Wang T, Li Y, Chen H, Fu Q, Zhang H, Wang B. Li X, et al. Among authors: wang t, wang b. J Med Genet. 2020 May 6:jmedgenet-2019-106608. doi: 10.1136/jmedgenet-2019-106608. Online ahead of print. J Med Genet. 2020. PMID: 32376791

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