Found: 16
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Application of the Single-Molecule Real-Time Technology (SMRT) for Identification of HKαα Thalassemia Allele.
- Published in:
- Laboratory Medicine, 2023, v. 54, n. 1, p. 65, doi. 10.1093/labmed/lmac065
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- Article
Prenatal diagnosis of BACs‐on‐Beads assay in 1520 cases from Fujian Province, China.
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- Molecular Genetics & Genomic Medicine, 2020, v. 8, n. 10, p. 1, doi. 10.1002/mgg3.1446
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- Article
The clinical value of hsa-miR-190b-5p in peripheral blood of pediatric β-thalassemia and its regulation on BCL11A expression.
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- PLoS ONE, 2023, v. 18, n. 10, p. 1, doi. 10.1371/journal.pone.0292031
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- Article
Application of the prenatal BACs-on-Beads™ assay for rapid prenatal detection of sex chromosome mosaicism.
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- Molecular Genetics & Genomics, 2022, v. 297, n. 5, p. 1423, doi. 10.1007/s00438-022-01931-0
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- Article
Intelligent control using multiple neural networks.
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- International Journal of Adaptive Control & Signal Processing, 2003, v. 17, n. 6, p. 417, doi. 10.1002/acs.759
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- Article
Clinical findings and genetic analysis of patients with copy number variants involving 17p13.3 using a single nucleotide polymorphism array: a single-center experience.
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- BMC Medical Genomics, 2022, v. 15, n. 1, p. 1, doi. 10.1186/s12920-022-01423-5
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- Article
Prenatal genetic diagnosis of fetuses with dextrocardia using whole exome sequencing in a tertiary center.
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- Scientific Reports, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41598-024-67164-w
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- Article
Application of the BACs‐on‐Beads™ assay for rapid prenatal detection application of BoBs™ for PND of aneuploidies and microdeletions.
- Published in:
- Molecular Reproduction & Development, 2018, v. 85, n. 2, p. 146, doi. 10.1002/mrd.22945
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- Article
A novel PLS1 c.981+1G>A variant causes autosomal‐dominant hereditary hearing loss in a family.
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- Clinical Genetics, 2023, v. 103, n. 4, p. 413, doi. 10.1111/cge.14283
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- Article
Molecular analysis and prenatal diagnosis of seven Chinese families with genetic epilepsy.
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- Frontiers in Neuroscience, 2023, p. 1, doi. 10.3389/fnins.2023.1165601
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- Article
Analysis of genotype-phenotype correlation in patients with α-thalassemia from Fujian province, Southeastern China.
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- 2022
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- journal article
Genetic research and clinical analysis of β‐globin gene cluster deletions in the Chinese population of Fujian province: A 14‐year single‐center experience.
- Published in:
- Journal of Clinical Laboratory Analysis, 2022, v. 36, n. 2, p. 1, doi. 10.1002/jcla.24181
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- Article
Prenatal diagnosis of thalassemia in 695 pedigrees from southeastern China: a 10-year follow-up study.
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- 2021
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- journal article
First report of the spectrum of δ‐globin gene mutations among women of reproductive age in Fujian area—Discrimination of δ‐thalassemia, α‐thalassemia, and Iron Deficiency Anemia.
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- Journal of Clinical Laboratory Analysis, 2020, v. 34, n. 11, p. 1, doi. 10.1002/jcla.23479
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- Article
X-linked ichthyosis: Molecular findings in four pedigrees with inconspicuous clinical manifestations.
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- 2020
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- journal article
Molecular characterization of thalassemia and hemoglobinopathy in Southeastern China.
- Published in:
- Scientific Reports, 2019, v. 9, n. 1, p. 1, doi. 10.1038/s41598-019-40089-5
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- Article