Found: 17
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The value of <sup>68</sup>Ga-PSMA PET/CT in the diagnosis of intracapsular prostate cancer with a poor prognosis.
- Published in:
- Discover Oncology, 2024, v. 15, n. 1, p. 1, doi. 10.1007/s12672-024-01127-5
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- Publication type:
- Article
Insurance Reimbursement for Special Foods and Phenylalanine Levels in Patients With PKU in China.
- Published in:
- JAMA Network Open, 2024, v. 7, n. 6, p. e2412886, doi. 10.1001/jamanetworkopen.2024.12886
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- Publication type:
- Article
Anlotinib for Metastatic Progressed Pheochromocytoma and Paraganglioma: A Retrospective Study of Real-World Data.
- Published in:
- Journal of the Endocrine Society, 2024, v. 8, n. 6, p. 1, doi. 10.1210/jendso/bvae061
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- Publication type:
- Article
A Mettl16/m<sup>6</sup>A/mybl2b/Igf2bp1 axis ensures cell cycle progression of embryonic hematopoietic stem and progenitor cells.
- Published in:
- EMBO Journal, 2024, v. 43, n. 10, p. 1990, doi. 10.1038/s44318-024-00082-9
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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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- Publication type:
- 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
A feasibility study of noninvasive prenatal diagnosis in facioscapulohumeral muscular dystrophy type 1 in a Chinese family.
- Published in:
- Frontiers in Genetics, 2022, v. 13, p. 1, doi. 10.3389/fgene.2022.1046096
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- Publication type:
- Article
Genetic deconvolution of fetal and maternal cell-free DNA in maternal plasma enables next-generation non-invasive prenatal screening.
- Published in:
- Cell Discovery, 2022, v. 8, n. 1, p. 1, doi. 10.1038/s41421-022-00457-4
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- Publication type:
- Article
Incidence of Down Syndrome by maternal age in Chinese population.
- Published in:
- Frontiers in Genetics, 2022, v. 13, p. 01, doi. 10.3389/fgene.2022.980627
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- Publication type:
- Article
Prenatal diagnosis and genetic counseling of a 10p11.23q11.21 duplication associated with normal phenotype.
- Published in:
- 2022
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- Publication type:
- Case Study
Genomic architecture of fetal central nervous system anomalies using whole-genome sequencing.
- Published in:
- NPJ Genomic Medicine, 2022, v. 7, n. 1, p. 1, doi. 10.1038/s41525-022-00301-4
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- Publication type:
- Article
Clinical efficiency of simultaneous CNV-seq and whole-exome sequencing for testing fetal structural anomalies.
- Published in:
- 2022
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- Publication type:
- journal article
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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- 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
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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- Publication type:
- Article
Two Novel Mutations in the C-Terminal Region of Centrosomal Protein 290 (CEP290) Result in Classic Joubert Syndrome.
- Published in:
- Journal of Child Neurology, 2015, v. 30, n. 6, p. 772, doi. 10.1177/0883073814535488
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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.
- Published in:
- Molecular Cytogenetics (17558166), 2014, v. 7, n. 1, p. 1, doi. 10.1186/s13039-014-0062-y
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- Publication type:
- Article