Search Page
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
Filters
Results by year
Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2020 | 1 |
2021 | 2 |
2022 | 2 |
2023 | 3 |
2024 | 0 |
Search Results
6 results
Results by year
Filters applied: . Clear all
Page 1
Ndufa4 Regulates the Proliferation and Apoptosis of Neurons via miR-145a-5p/Homer1/Ccnd2.
Mol Neurobiol. 2023 Jun;60(6):2986-3003. doi: 10.1007/s12035-023-03239-5. Epub 2023 Feb 10.
Mol Neurobiol. 2023.
PMID: 36763283
Free PMC article.
Prenatal diagnosis of Williams-Beuren syndrome by ultrasound and chromosomal microarray analysis.
Huang R, Zhou H, Fu F, Li R, Lei T, Li Y, Cheng K, Wang Y, Yang X, Li L, Jing X, Zhang Y, Li F, Li D, Liao C.
Huang R, et al.
Mol Cytogenet. 2022 Jun 28;15(1):27. doi: 10.1186/s13039-022-00604-2.
Mol Cytogenet. 2022.
PMID: 35765027
Free PMC article.
Item in Clipboard
Whole exome sequencing improves genetic diagnosis of fetal clubfoot.
Huang R, Zhou H, Ma C, Fu F, Cheng K, Wang Y, Li R, Lei T, Yu Q, Wang D, Yan S, Yang X, Li D, Liao C.
Huang R, et al.
Hum Genet. 2023 Mar;142(3):407-418. doi: 10.1007/s00439-022-02516-y. Epub 2022 Dec 25.
Hum Genet. 2023.
PMID: 36566310
Item in Clipboard
Prenatal diagnosis in the fetal hyperechogenic kidneys: assessment using chromosomal microarray analysis and exome sequencing.
Huang R, Fu F, Zhou H, Zhang L, Lei T, Cheng K, Yan S, Guo F, Wang Y, Ma C, Li R, Yu Q, Deng Q, Li L, Yang X, Han J, Li D, Liao C.
Huang R, et al.
Hum Genet. 2023 Jun;142(6):835-847. doi: 10.1007/s00439-023-02545-1. Epub 2023 Apr 24.
Hum Genet. 2023.
PMID: 37095353
Review.
Item in Clipboard
[Analysis of families with fetal congenital abnormalities but negative prenatal diagnosis by whole exome sequencing].
Fu F, Li LS, Du K, Li R, Yu QX, Wang D, Lei TY, Deng Q, Nie ZQ, Zhang WW, Yang X, Han J, Zhen L, Pan M, Zhang LN, Li FC, Zhang YL, Jing XY, Li DZ, Liao C.
Fu F, et al.
Zhonghua Fu Chan Ke Za Zhi. 2021 Jul 25;56(7):458-466. doi: 10.3760/cma.j.cn112141-20210118-00028.
Zhonghua Fu Chan Ke Za Zhi. 2021.
PMID: 34304437
Chinese.
Item in Clipboard
Compound heterozygous mutation of the ASXL3 gene causes autosomal recessive congenital heart disease.
Fu F, Li R, Lei TY, Wang D, Yang X, Han J, Pan M, Zhen L, Li J, Li FT, Jing XY, Li DZ, Liao C.
Fu F, et al.
Hum Genet. 2021 Feb;140(2):333-348. doi: 10.1007/s00439-020-02200-z. Epub 2020 Jul 21.
Hum Genet. 2021.
PMID: 32696347
Item in Clipboard
Cite
Cite