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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2023 | 4 |
2024 | 3 |
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6 results
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Page 1
Noninvasive twin genotyping for recessive monogenic disorders by relative haplotype dosage.
Prenat Diagn. 2024 Apr 22. doi: 10.1002/pd.6565. Online ahead of print.
Prenat Diagn. 2024.
PMID: 38647204
First-trimester noninvasive prenatal diagnosis of seven facioscapulohumeral muscular dystrophy type 1 families using SNP-based amplicon sequencing: An earlier, rapid and safer way.
Fu X, Zhao Z, Kong L, Li S, Li F, Han X, Sun L, Wu D, Wang Y, Kong X.
Fu X, et al.
Am J Med Genet A. 2024 Jun;194(6):e63560. doi: 10.1002/ajmg.a.63560. Epub 2024 Feb 8.
Am J Med Genet A. 2024.
PMID: 38329169
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Prenatal diagnosis of 1408 foetuses at risk of DMD/BMD by MLPA and Sanger sequencing combined with STR linkage analysis.
Hua C, Liu L, Kong X.
Hua C, et al.
BMC Med Genomics. 2023 Dec 1;16(1):310. doi: 10.1186/s12920-023-01746-x.
BMC Med Genomics. 2023.
PMID: 38041114
Free PMC article.
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Haplotype-based noninvasive prenatal diagnosis of methylmalonic acidemia and the discovery of a recurrent pathogenic haplotype associated with c.609G>A.
Fu X, Li S, Zhao Z, Kong L, Zhu J, Li H, Feng J, Tang W, Wu D, Kong X.
Fu X, et al.
Prenat Diagn. 2023 Nov;43(12):1544-1555. doi: 10.1002/pd.6458. Epub 2023 Nov 13.
Prenat Diagn. 2023.
PMID: 37957774
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Exploring factors impacting haplotype-based noninvasive prenatal diagnosis for single-gene recessive disorders.
Kong L, Li S, Zhao Z, Feng J, Fu X, Li H, Zhu J, Wang Y, Tang W, Yuan C, Li F, Han X, Wu D, Kong X, Sun L.
Kong L, et al.
Clin Genet. 2024 Jan;105(1):52-61. doi: 10.1111/cge.14434. Epub 2023 Oct 11.
Clin Genet. 2024.
PMID: 37822034
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Whole-exome sequencing in deceased fetuses with ultrasound anomalies: a retrospective analysis.
Huang W, Zhu X, Sun G, Gao Z, Kong X.
Huang W, et al.
BMC Med Genomics. 2023 Feb 16;16(1):25. doi: 10.1186/s12920-022-01427-1.
BMC Med Genomics. 2023.
PMID: 36797717
Free PMC article.
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