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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2004 1
2005 3
2006 11
2007 13
2008 17
2009 24
2010 19
2011 13
2012 18
2013 12
2014 22
2015 23
2016 30
2017 30
2018 32
2019 47
2020 43
2021 57
2022 79
2023 77
2024 18

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489 results

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Page 1
Application of exome sequencing for prenatal diagnosis of fetal structural anomalies: clinical experience and lessons learned from a cohort of 1618 fetuses.
Fu F, Li R, Yu Q, Wang D, Deng Q, Li L, Lei T, Chen G, Nie Z, Yang X, Han J, Pan M, Zhen L, Zhang Y, Jing X, Li F, Li F, Zhang L, Yi C, Li Y, Lu Y, Zhou H, Cheng K, Li J, Xiang L, Zhang J, Tang S, Fang P, Li D, Liao C. Fu F, et al. Among authors: li d. Genome Med. 2022 Oct 28;14(1):123. doi: 10.1186/s13073-022-01130-x. Genome Med. 2022. PMID: 36307859 Free PMC article.
Invasive prenatal diagnosis of fetal thalassemia.
Li DZ, Yang YD. Li DZ, et al. Best Pract Res Clin Obstet Gynaecol. 2017 Feb;39:41-52. doi: 10.1016/j.bpobgyn.2016.10.011. Epub 2016 Oct 26. Best Pract Res Clin Obstet Gynaecol. 2017. PMID: 27889305 Review.
PDIA2 variant associated with vitiligo.
Li F, Liao C, Li R, Zhang Y, Jing X, Li D, Deng W. Li F, et al. Among authors: li d. Skin Health Dis. 2023 Aug 16;3(5):e278. doi: 10.1002/ski2.278. eCollection 2023 Oct. Skin Health Dis. 2023. PMID: 37799362 Free PMC article.
Prenatal Diagnosis of Chromosome 16p11.2 Microdeletion.
Wang Y, Zhou H, Fu F, Cheng K, Yu Q, Huang R, Lei T, Yang X, Li D, Liao C. Wang Y, et al. Among authors: li d. Genes (Basel). 2022 Dec 8;13(12):2315. doi: 10.3390/genes13122315. Genes (Basel). 2022. PMID: 36553582 Free PMC article.
Placenta insufficiency and congenital heart defects.
Pan M, Li DZ. Pan M, et al. Am J Obstet Gynecol MFM. 2023 Sep;5(9):101070. doi: 10.1016/j.ajogmf.2023.101070. Epub 2023 Jul 3. Am J Obstet Gynecol MFM. 2023. PMID: 37406988 No abstract available.
Unexplained severe polyhydramnios: Remember Bartter syndrome.
Chen GL, Wen YJ, Li DZ. Chen GL, et al. Eur J Obstet Gynecol Reprod Biol. 2023 Apr;283:171-172. doi: 10.1016/j.ejogrb.2023.02.011. Epub 2023 Feb 14. Eur J Obstet Gynecol Reprod Biol. 2023. PMID: 36803950 No abstract available.
Exome sequencing improves genetic diagnosis of congenital orofacial clefts.
Yan S, Fu F, Li R, Yu Q, Li F, Zhou H, Wang Y, Huang R, Ma C, Guo F, Wang D, Yang X, Han J, Lei T, Li D, Liao C. Yan S, et al. Among authors: li d. Front Genet. 2023 Sep 7;14:1252823. doi: 10.3389/fgene.2023.1252823. eCollection 2023. Front Genet. 2023. PMID: 37745857 Free PMC article.
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. Among authors: li d. Hum Genet. 2023 Mar;142(3):407-418. doi: 10.1007/s00439-022-02516-y. Epub 2022 Dec 25. Hum Genet. 2023. PMID: 36566310
Genetic diagnosis of fetal microcephaly at a single tertiary center in China.
Wang Y, Fu F, Lei T, Zhen L, Deng Q, Zhou H, Ma C, Cheng K, Huang R, Li R, Yu Q, Li L, Han J, Yang X, Li D, Liao C. Wang Y, et al. Among authors: li d. Front Genet. 2023 May 9;14:1112153. doi: 10.3389/fgene.2023.1112153. eCollection 2023. Front Genet. 2023. PMID: 37229200 Free PMC article.
489 results