Found: 16
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Retrospective study revealed integration of CNV-seq and karyotype analysis is an effective strategy for prenatal diagnosis of chromosomal abnormalities.
- Published in:
- Frontiers in Genetics, 2024, p. 01, doi. 10.3389/fgene.2024.1387724
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- Article
Epidemiology of human papillomavirus infection in women from Xiamen, China, 2013 to 2023.
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- Frontiers in Public Health, 2024, p. 1, doi. 10.3389/fpubh.2024.1332696
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- Article
THE VALUE OF NIPT COMBINED WITH SERUM CELL-FREE DNA, ESTRIOL, AFP, AND β-HCG LEVELS IN THE RECOGNITION OF TRISOMY 21 AND 18 IN THE SECOND TRIMESTER.
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- Journal of Medical Biochemistry, 2023, v. 42, n. 4, p. 574, doi. 10.5937/jomb0-33027
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- Article
Prevalence and genotype distribution of HPV infection among women in Xiamen, China.
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- Frontiers in Microbiology, 2023, p. 1, doi. 10.3389/fmicb.2023.1130226
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- Article
Evaluation of strategies for identification of infants with pathogenic glucose-6-phosphate dehydrogenase variants in China.
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- Frontiers in Genetics, 2022, v. 13, p. 01, doi. 10.3389/fgene.2022.844381
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- Article
Prenatal Genetic Diagnosis of Fetal Cystic Hygroma: A Retrospective Single-Center Study from China.
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- Cytogenetic & Genome Research, 2022, v. 162, n. 7, p. 354, doi. 10.1159/000528600
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- Article
Clinical Characteristics, In Silico Analysis, and Intervention of Neonatal-Onset Inflammatory Bowel Disease With Combined Immunodeficiency Caused by Novel TTC7A Variants.
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- 2022
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- Case Study
The expression and prognostic value of minichromosome maintenance markers in human breast cancer: a comprehensive analysis.
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- European Journal of Gynaecological Oncology, 2022, v. 43, n. 2, p. 227, doi. 10.31083/j.ejgo4302029
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- Article
Newborn Screening for G6PD Deficiency in Xiamen, China: Prevalence, Variant Spectrum, and Genotype-Phenotype Correlations.
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- Frontiers in Genetics, 2021, v. 12, p. 1, doi. 10.3389/fgene.2021.718503
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- Article
A Novel de novo Mutation in EBF3 Associated With Hypotonia, Ataxia, and Delayed Development Syndrome in a Chinese Boy.
- Published in:
- Frontiers in Genetics, 2021, v. 12, p. 1, doi. 10.3389/fgene.2021.676832
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- Article
Expanded noninvasive prenatal testing for fetal aneuploidy and copy number variations and parental willingness for invasive diagnosis in a cohort of 18,516 cases.
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- BMC Medical Genomics, 2021, v. 14, n. 1, p. 1, doi. 10.1186/s12920-021-00955-6
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- Article
A familial analysis of two brothers with azoospermia caused by maternal 46,Y, t(X; 1) (q28; q21) chromosomal abnormality.
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- Andrologia, 2021, v. 53, n. 1, p. 1, doi. 10.1111/and.13867
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- Article
Pedigree analysis of two brothers with severe oligozoospermia caused by maternal inv(X) (p22.3, q22) chromosome abnormality.
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- Andrologia, 2020, v. 52, n. 6, p. 1, doi. 10.1111/and.13602
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- Article
Spray-painted human fibronectin coating as an effective strategy to enhance graft ligamentization of a polyethylene terephthalate artificial ligament.
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- Biotechnology Letters, 2014, v. 36, n. 5, p. 1079, doi. 10.1007/s10529-013-1447-4
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- Article
Enhancement of the osseointegration of a polyethylene terephthalate artificial ligament graft in a bone tunnel using 58S bioglass.
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- International Orthopaedics, 2012, v. 36, n. 1, p. 191, doi. 10.1007/s00264-011-1275-x
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- Article
Hydroxyapatite coating enhances polyethylene terephthalate artificial ligament graft osseointegration in the bone tunnel.
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- International Orthopaedics, 2011, v. 35, n. 10, p. 1561, doi. 10.1007/s00264-010-1158-6
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- Publication type:
- Article