Found: 11
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Identification of a Novel NOG Missense Mutation in a Chinese Family With Symphalangism and Tarsal Coalitions.
- Published in:
- Frontiers in Genetics, 2019, p. N.PAG, doi. 10.3389/fgene.2019.00353
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- Article
A Novel SPAST Mutation Results in Spastin Accumulation and Defects in Microtubule Dynamics.
- Published in:
- Movement Disorders, 2022, v. 37, n. 3, p. 598, doi. 10.1002/mds.28885
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- Article
Case Report: Identification of a novel CASK missense variant in a Chinese family with MICPCH.
- Published in:
- 2022
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- Case Study
Decidual vascular endothelial cells promote maternal-fetal immune tolerance by inducing regulatory T cells through canonical Notch1 signaling.
- Published in:
- Immunology & Cell Biology, 2017, v. 95, n. 4, p. 416, doi. 10.1038/icb.2017.12
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- Article
Decidual vascular endothelial cells promote maternal-fetal immune tolerance by inducing regulatory T cells through canonical Notch1 signaling.
- Published in:
- Immunology & Cell Biology, 2016, v. 94, n. 5, p. 458, doi. 10.1038/icb.2015.119
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- Article
Prenatal diagnosis and outcomes in 320 fetuses with nasal bone anomalies.
- Published in:
- Frontiers in Genetics, 2023, p. 1, doi. 10.3389/fgene.2023.1170720
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- Publication type:
- Article
Prenatal Detection of Novel Compound Heterozygous Splice Site Variants of the KIAA0825 Gene in a Fetus with Postaxial Polydactyly Type A.
- Published in:
- Genes, 2022, v. 13, n. 7, p. 1230, doi. 10.3390/genes13071230
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- Article
Numerical investigation on the exhaust gas combustion of an SOFC in a catalytic multichannel burner.
- Published in:
- Frontiers in Energy Research, 2024, p. 01, doi. 10.3389/fenrg.2024.1322956
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- Publication type:
- Article
A family with Robertsonian translocation: a potential mechanism of speciation in humans.
- Published in:
- Molecular Cytogenetics (17558166), 2016, v. 9, p. 1, doi. 10.1186/s13039-016-0255-7
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- Publication type:
- Article
Prenatal diagnosis of a de novo interstitial deletion of 11q (11q22.3 → q23.3) associated with abnormal ultrasound findings by array comparative genomic hybridization.
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- Molecular Cytogenetics (17558166), 2014, v. 7, n. 1, p. 1, doi. 10.1186/s13039-014-0062-y
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- Publication type:
- Article
Prenatal whole-exome sequencing for fetal structural anomalies: a retrospective analysis of 145 Chinese cases.
- Published in:
- BMC Medical Genomics, 2023, v. 16, n. 1, p. 1, doi. 10.1186/s12920-023-01697-3
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- Article