Found: 31
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Constitutive Expression of Adiponectin in Endothelial Progenitor Cells Protects a Rat Model of Cerebral Ischemia.
- Published in:
- Neural Plasticity, 2017, p. 1, doi. 10.1155/2017/6809745
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- Article
Fetal mosaicism, should conventional karyotype always be performed?
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- Journal of Obstetrics & Gynaecology Research, 2023, v. 49, n. 12, p. 2836, doi. 10.1111/jog.15804
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- Article
Using single nucleotide polymorphism array for prenatal diagnosis in a large multicenter study in Southern China.
- Published in:
- Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-33668-0
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- Article
Association of hemoglobin-to-red cell distribution width ratio with the three-month outcomes in patients with acute ischemic stroke.
- Published in:
- Frontiers in Neurology, 2024, p. 1, doi. 10.3389/fneur.2024.1425633
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- Article
Fetal growth restriction: associated genetic etiology and pregnancy outcomes in a tertiary referral center.
- Published in:
- 2022
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- Publication type:
- journal article
Prenatal diagnosis of non-mosaic sex chromosome abnormalities: a 10-year experience from a tertiary referral center.
- Published in:
- Journal of Perinatal Medicine, 2023, v. 51, n. 7, p. 904, doi. 10.1515/jpm-2022-0552
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- Article
Evaluation of genetic variants using chromosomal microarray analysis for fetuses with polyhydramnios.
- Published in:
- BMC Medical Genomics, 2022, v. 15, n. 1, p. 1, doi. 10.1186/s12920-022-01224-w
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- Article
Comprehensive analysis of early pregnancy loss based on cytogenetic findings from a tertiary referral center.
- Published in:
- Molecular Cytogenetics (17558166), 2021, v. 14, n. 1, p. 1, doi. 10.1186/s13039-021-00577-8
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- Article
Copy number variations associated with fetal congenital kidney malformations.
- Published in:
- Molecular Cytogenetics (17558166), 2020, v. 13, n. 1, p. 1, doi. 10.1186/s13039-020-00481-7
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- Publication type:
- Article
Submicroscopic aberrations of chromosome 16 in prenatal diagnosis.
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- Molecular Cytogenetics (17558166), 2019, v. 12, n. 1, p. N.PAG, doi. 10.1186/s13039-019-0448-y
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- Publication type:
- Article
Chromosomal abnormalities and copy number variations in fetal ventricular septal defects.
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- Molecular Cytogenetics (17558166), 2018, v. 11, n. 1, p. N.PAG, doi. 10.1186/s13039-018-0408-y
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- Publication type:
- Article
Single nucleotide polymorphism array (SNP-array) analysis for fetuses with abnormal nasal bone.
- Published in:
- Archives of Gynecology & Obstetrics, 2024, v. 309, n. 6, p. 2475, doi. 10.1007/s00404-023-07122-5
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- Publication type:
- Article
Downregulation of miR-146b-3p Inhibits Proliferation and Migration and Modulates the Expression and Location of Sodium/Iodide Symporter in Dedifferentiated Thyroid Cancer by Potentially Targeting MUC20.
- Published in:
- Frontiers in Oncology, 2021, v. 11, p. N.PAG, doi. 10.3389/fonc.2020.566365
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- Article
Choroid Plexus Cysts: Single Nucleotide Polymorphism Array Analysis of Associated Genetic Anomalies and Resulting Obstetrical Outcomes.
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- Risk Management & Healthcare Policy, 2021, n. 14, p. 2491, doi. 10.2147/RMHP.S312813
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- Article
Prenatal diagnosis of Pallister‐Killian syndrome and literature review.
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- Journal of Cellular & Molecular Medicine, 2021, v. 25, n. 18, p. 8929, doi. 10.1111/jcmm.16853
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- Article
Chromosomal microarray analysis for pregnancies with abnormal maternal serum screening who undergo invasive prenatal testing.
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- Journal of Cellular & Molecular Medicine, 2021, v. 25, n. 13, p. 6271, doi. 10.1111/jcmm.16589
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- Publication type:
- Article
Time-variant fragility analysis of the bridge system considering time-varying dependence among typical component seismic demands.
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- Earthquake Engineering & Engineering Vibration, 2019, v. 18, n. 2, p. 363, doi. 10.1007/s11803-019-0509-6
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- Publication type:
- Article
A Dynamic Propagation Numerical Model of Hydraulic Fracture Interactions with Pre-Existing Complex Natural Fractures.
- Published in:
- Processes, 2024, v. 12, n. 5, p. 899, doi. 10.3390/pr12050899
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- Publication type:
- Article
Different Cutoff Values for Increased Nuchal Translucency in First-Trimester Screening to Predict Fetal Chromosomal Abnormalities.
- Published in:
- International Journal of General Medicine, 2021, v. 14, p. 8437, doi. 10.2147/IJGM.S330960
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- Publication type:
- Article
Application of Single Nucleotide Polymorphism Microarray in Prenatal Diagnosis of Fetuses with Central Nervous System Abnormalities.
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- International Journal of General Medicine, 2021, v. 14, p. 4239, doi. 10.2147/IJGM.S323899
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- Publication type:
- Article
Study on rock fracture mechanism and hydraulic fracturing propagation law of heterogeneous tight sandstone reservoir.
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- PLoS ONE, 2024, v. 19, n. 8, p. 1, doi. 10.1371/journal.pone.0303251
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- Publication type:
- Article
Prenatal diagnosis and genetic etiology analysis of talipes equinovarus by chromosomal microarray analysis.
- Published in:
- BMC Medical Genomics, 2023, v. 16, n. 1, p. 1, doi. 10.1186/s12920-023-01733-2
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- Publication type:
- Article
Chromosomal Microarray Analysis for the Fetuses with Aortic Arch Abnormalities and Normal Karyotype.
- Published in:
- Molecular Diagnosis & Therapy, 2020, v. 24, n. 5, p. 611, doi. 10.1007/s40291-020-00474-7
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- Publication type:
- Article
Robust Control Design for an Uncertain Macroeconomic Dynamical System with Unknown Characteristics and Inequality Control Constraint.
- Published in:
- Complexity, 2021, p. 1, doi. 10.1155/2021/8826480
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- Publication type:
- Article
Chromosomal microarray analysis for pregnancies with or without ultrasound abnormalities in women of advanced maternal age.
- Published in:
- 2020
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- Publication type:
- journal article
Detection of copy number disorders associated with congenital anomalies of the kidney and urinary tract in fetuses via single nucleotide polymorphism arrays.
- Published in:
- 2020
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- Publication type:
- journal article
Clinical application of chromosomal microarray analysis in fetuses with increased nuchal translucency and normal karyotype.
- Published in:
- Molecular Genetics & Genomic Medicine, 2019, v. 7, n. 8, p. N.PAG, doi. 10.1002/mgg3.811
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- Publication type:
- Article
Copy number variations in ultrasonically abnormal late pregnancy fetuses with normal karyotypes.
- Published in:
- Scientific Reports, 2020, v. 10, n. 1, p. N.PAG, doi. 10.1038/s41598-020-72157-6
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- Publication type:
- Article
Use of mouse primary epidermal organoids for USA300 infection modeling and drug screening.
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- Cell Death & Disease, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41419-022-05525-x
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- Publication type:
- Article
Red Cell Distribution Width-to-Platelet Count Ratio: A Promising Predictor of In-Hospital All-Cause Mortality in Critically Ill Patients with Acute Ischemic Stroke.
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- Cerebrovascular Diseases, 2023, v. 52, n. 6, p. 692, doi. 10.1159/000529184
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- Article
Prenatal diagnosis of 22q11.2 copy number abnormalities in fetuses via single nucleotide polymorphism array.
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- Molecular Biology Reports, 2020, v. 47, n. 10, p. 7529, doi. 10.1007/s11033-020-05815-7
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- Publication type:
- Article