Li F - Search Results

1

Contribution of maternal mosaicism to false-positive chromosome X loss associated with noninvasive prenatal testing.

Wan J, Li R, Li F, Yu Q, Wang D, Sun X, Zhang Y, Jing X, Tang X, Chen G, Jiang F, Li F, Fu F, Li Y, Zhang L, Yi C, Li J, Li D, Liao C. Wan J, et al. Among authors: li f, li d, li y, li j, li r. J Matern Fetal Neonatal Med. 2022 Dec;35(25):9647-9653. doi: 10.1080/14767058.2022.2050362. Epub 2022 Mar 13. J Matern Fetal Neonatal Med. 2022. PMID: 35282756 Free article.

2

Pregnancy outcome of autosomal aneuploidies other than common trisomies detected by noninvasive prenatal testing in routine clinical practice.

Wan J, Li R, Zhang Y, Jing X, Yu Q, Li F, Li Y, Zhang L, Yi C, Li J, Li D, Liao C. Wan J, et al. Among authors: li f, li d, li y, li j, li r. Prenat Diagn. 2018 Oct;38(11):849-857. doi: 10.1002/pd.5340. Epub 2018 Sep 6. Prenat Diagn. 2018. PMID: 30078205

3

Prenatal diagnosis of submicroscopic chromosomal aberrations in fetuses with congenital cystic adenomatoid malformation by chromosomal microarray analysis.

Deng Q, Huang L, Liu J, Fang F, Liu Z, Zhang Y, Li F, Liao C. Deng Q, et al. Among authors: li f. J Matern Fetal Neonatal Med. 2021 Aug;34(16):2623-2629. doi: 10.1080/14767058.2019.1670793. Epub 2019 Oct 3. J Matern Fetal Neonatal Med. 2021. PMID: 31581877 Free article.

4

Prenatal exome sequencing in fetuses with congenital heart defects.

Li R, Fu F, Yu Q, Wang D, Jing X, Zhang Y, Li F, Li F, Han J, Pan M, Zhen L, Li D, Liao C. Li R, et al. Among authors: li f, li d. Clin Genet. 2020 Sep;98(3):215-230. doi: 10.1111/cge.13774. Epub 2020 Jun 9. Clin Genet. 2020. PMID: 32410215

5

Prenatal diagnosis of 21 fetuses with balanced chromosomal abnormalities (BCAs) using whole-genome sequencing.

Fu F, Li R, Dang X, Yu Q, Xu K, Gu W, Wang D, Yang X, Pan M, Zhen L, Zhang Y, Li F, Jing X, Li F, Li D, Liao C. Fu F, et al. Among authors: li f, li d, li r. Front Genet. 2022 Sep 15;13:951829. doi: 10.3389/fgene.2022.951829. eCollection 2022. Front Genet. 2022. PMID: 36186435 Free PMC article.

6

Chromosome microarray analysis in the investigation of children with congenital heart disease.

Wu XL, Li R, Fu F, Pan M, Han J, Yang X, Zhang YL, Li FT, Liao C. Wu XL, et al. Among authors: li ft, li r. BMC Pediatr. 2017 May 4;17(1):117. doi: 10.1186/s12887-017-0863-3. BMC Pediatr. 2017. PMID: 28472932 Free PMC article. Clinical Trial.

7

Prenatal diagnosis of trisomy 18 rescue resulting in mosaic of two different diploid cell lines in a hydropic fetus.

Deng Q, Li R, Fu F, Li FT, Jing XY, Liao C. Deng Q, et al. Among authors: li ft, li r. Eur J Obstet Gynecol Reprod Biol. 2018 May;224:209-211. doi: 10.1016/j.ejogrb.2018.04.005. Epub 2018 Apr 6. Eur J Obstet Gynecol Reprod Biol. 2018. PMID: 29653728 No abstract available.

8

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. Among authors: li ft, li j, li dz, li r. Hum Genet. 2021 Feb;140(2):333-348. doi: 10.1007/s00439-020-02200-z. Epub 2020 Jul 21. Hum Genet. 2021. PMID: 32696347

9

Insufficient fetal fraction of cell-free DNA in non-invasive prenatal testing: Not always true.

Wan JH, Li FT, Li R, Zhong HZ, Li DZ. Wan JH, et al. Eur J Obstet Gynecol Reprod Biol. 2021 Jun;261:245-247. doi: 10.1016/j.ejogrb.2021.04.026. Epub 2021 Apr 21. Eur J Obstet Gynecol Reprod Biol. 2021. PMID: 33910769 No abstract available.

10

A novel SPTB frameshift deletion causing hereditary spherocytosis identified by next-generation sequencing in a Chinese family.

Zhao RQ, Jiang F, Li J, Zhou JY, Tang XW, Li FT, Chen LQ, Li DZ. Zhao RQ, et al. Among authors: li ft, li j, li dz. Int J Lab Hematol. 2021 Dec;43(6):e294-e297. doi: 10.1111/ijlh.13575. Epub 2021 May 11. Int J Lab Hematol. 2021. PMID: 33974364 No abstract available.

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