Found: 23
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Association of a unicornuate uterus with adverse obstetric outcomes: A retrospective cohort study.
- Published in:
- Journal of Obstetrics & Gynaecology Research, 2021, v. 47, n. 9, p. 3136, doi. 10.1111/jog.14911
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- Publication type:
- Article
A Rapid PCR-Free Next-Generation Sequencing Method for the Detection of Copy Number Variations in Prenatal Samples.
- Published in:
- Life (2075-1729), 2021, v. 11, n. 2, p. 98, doi. 10.3390/life11020098
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- Publication type:
- Article
Spontaneous Resolution of a Fetal Dural Sinus Thrombosis: One Case Report and Review of the Literatures.
- Published in:
- 2012
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- Publication type:
- Case Study
Recognition of uterine contractions with electrohysterogram and exploring the best electrode combination.
- Published in:
- 2022
- By:
- Publication type:
- journal article
Factors associated with test failure in pregnant women undergoing cell-free DNA-based testing for fetal trisomy.
- Published in:
- Journal of Medical Screening, 2021, v. 28, n. 4, p. 411, doi. 10.1177/09691413211009940
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- Publication type:
- Article
Isobaric tag for relative and absolute quantitation based quantitative proteomics reveals unique urinary protein profiles in patients with preeclampsia.
- Published in:
- Journal of Cellular & Molecular Medicine, 2019, v. 23, n. 8, p. 5822, doi. 10.1111/jcmm.14459
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- Publication type:
- Article
Assessment of Features between Multichannel Electrohysterogram for Differentiation of Labors.
- Published in:
- Sensors (14248220), 2022, v. 22, n. 9, p. 3352, doi. 10.3390/s22093352
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- Publication type:
- Article
Preliminary Study on the Efficient Electrohysterogram Segments for Recognizing Uterine Contractions with Convolutional Neural Networks.
- Published in:
- BioMed Research International, 2019, p. 1, doi. 10.1155/2019/3168541
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- Publication type:
- Article
Prenatal diagnosis of recurrent Kagami–Ogata syndrome inherited from a mother affected by Temple syndrome: a case report and literature review.
- Published in:
- BMC Medical Genomics, 2024, v. 17, n. 1, p. 1, doi. 10.1186/s12920-024-01987-4
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- Publication type:
- Article
Prenatal genetic diagnosis of disseminated infantile myofibromatosis: a case report and literature review.
- Published in:
- BMC Medical Genomics, 2023, v. 16, n. 1, p. 1, doi. 10.1186/s12920-023-01612-w
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- Publication type:
- Article
Automatic recognition of uterine contractions with electrohysterogram signals based on the zero-crossing rate.
- Published in:
- Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-81492-1
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- Publication type:
- Article
High levels of circulating cell‐free DNA are a biomarker of active SLE.
- Published in:
- European Journal of Clinical Investigation, 2018, v. 48, n. 11, p. N.PAG, doi. 10.1111/eci.13015
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- Publication type:
- Article
A rare de novo duplication of chromosome 21q22.12?q22.3 with other concomitant deletion and duplication of small fragments in 21q associated with Down syndrome: Prenatal diagnosis, molecular cytogenetic characterization.
- Published in:
- Molecular Cytogenetics (17558166), 2013, v. 6, n. 1, p. 1, doi. 10.1186/1755-8166-6-11
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- Publication type:
- Article
Detection of Mosaic Absence of Heterozygosity (AOH) Using Low-Pass Whole Genome Sequencing in Prenatal Diagnosis: A Preliminary Report.
- Published in:
- Diagnostics (2075-4418), 2023, v. 13, n. 18, p. 2895, doi. 10.3390/diagnostics13182895
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- Publication type:
- Article
Evaluation and Analysis of Absence of Homozygosity (AOH) Using Chromosome Analysis by Medium Coverage Whole Genome Sequencing (CMA-seq) in Prenatal Diagnosis.
- Published in:
- Diagnostics (2075-4418), 2023, v. 13, n. 3, p. 560, doi. 10.3390/diagnostics13030560
- By:
- Publication type:
- Article
Contribution of maternal copy number variations to false-positive fetal trisomies detected by noninvasive prenatal testing.
- Published in:
- 2017
- By:
- Publication type:
- journal article
Copy number variation sequencing-based prenatal diagnosis using cell-free fetal DNA in amniotic fluid.
- Published in:
- 2016
- By:
- Publication type:
- journal article
Simultaneous Detection of CNVs and SNVs Improves the Diagnostic Yield of Fetuses with Ultrasound Anomalies and Normal Karyotypes.
- Published in:
- Genes, 2020, v. 11, n. 12, p. 1397, doi. 10.3390/genes11121397
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- Publication type:
- Article
Contribution of uniparental disomy to fetal growth restriction: a whole-exome sequencing series in a prenatal setting.
- Published in:
- Scientific Reports, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41598-023-50584-5
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- Publication type:
- Article
Development of Electrohysterogram Recording System for Monitoring Uterine Contraction.
- Published in:
- Journal of Healthcare Engineering, 2019, p. 1, doi. 10.1155/2019/4230157
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- Publication type:
- Article
Molten salt synthesis, characterization, and formation mechanism of superfine (Hf<sub>x</sub>Zr<sub>1‐x</sub>)B<sub>2</sub> solid‐solution powders.
- Published in:
- Journal of the American Ceramic Society, 2019, v. 102, n. 6, p. 3763, doi. 10.1111/jace.16246
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- Publication type:
- Article
Low‐temperature synthesis of ultrafine TiB<sub>2</sub> nanopowders by molten‐salt assisted borothermal reduction.
- Published in:
- Journal of the American Ceramic Society, 2018, v. 101, n. 12, p. 5299, doi. 10.1111/jace.15958
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- Publication type:
- Article
Synthesis of Ti<sub>0.2</sub>Zr<sub>0.8</sub>B<sub>2</sub> solid‐solution nanopowders by molten salt assisted borothermal reduction.
- Published in:
- Journal of the American Ceramic Society, 2018, v. 101, n. 11, p. 4899, doi. 10.1111/jace.15891
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- Publication type:
- Article