Works by Law, Hai Yang
Results: 24
An Isothermal Method for Whole Genome Amplification of Fresh and Degraded DNA for Comparative Genomic Hybridization, Genotyping and Mutation Detection.
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- DNA Research, 2006, v. 13, n. 2, p. 77, doi. 10.1093/dnares/dsi029
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- Article
Comment on: Severe β‐thalassemia (Hb Zunyi) mimicking congenital dyserythropoietic anemia—The deceivingly normal mean corpuscular volume and hemoglobin electrophoresis in dominantly inherited β‐thalassemia: Hb Little Venice.
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- Pediatric Blood & Cancer, 2024, v. 71, n. 11, p. 1, doi. 10.1002/pbc.31266
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- Article
Clinical application of targeted long read sequencing in prenatal beta‐thalassemia testing and genetic counseling.
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- 2024
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- Case Study
α-Thalassemia Mutations in Gilan Province, North Iran.
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- Hemoglobin, 2009, v. 33, n. 3/4, p. 235, doi. 10.1080/03630260903089029
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- Article
α-Thalassemia Mutation Analyses in Mazandaran Province, North Iran.
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- Hemoglobin, 2009, v. 33, n. 2, p. 115, doi. 10.1080/03630260902817297
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- Article
α-Thalassemia Mutations in Khuzestan Province, Southwest Iran.
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- Hemoglobin, 2008, v. 32, n. 6, p. 546, doi. 10.1080/03630260802532780
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- Article
FMR1 CGG Repeat Patterns and Flanking Haplotypes in Three Asian Populations and Their Relationship With Repeat Instability.
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- Annals of Human Genetics, 2006, v. 70, n. 6, p. 784, doi. 10.1111/j.1469-1809.2006.00265.x
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- Article
Use of capillary electrophoresis for thalassaemia screening.
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- Biomedical Chromatography, 1994, v. 8, n. 4, p. 175, doi. 10.1002/bmc.1130080406
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- Article
Degradation of methylation signals in cryopreserved DNA.
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- Clinical Epigenetics, 2023, v. 15, n. 1, p. 1, doi. 10.1186/s13148-023-01565-y
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- Article
Global DNA Hypermethylation in Down Syndrome Placenta.
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- PLoS Genetics, 2013, v. 9, n. 6, p. 1, doi. 10.1371/journal.pgen.1003515
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- Publication type:
- Article
Single-Tube Screen for Rapid Detection of Repeat Expansions in Seven Common Spinocerebellar Ataxias.
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- Clinical Chemistry, 2022, v. 68, n. 6, p. 794, doi. 10.1093/clinchem/hvac011
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- Article
An anemic patient with phenotypical β-thalassemic trait has elevated level of structurally normal β-globin mRNA in reticulocytes.
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- American Journal of Hematology, 2000, v. 65, n. 3, p. 243, doi. 10.1002/1096-8652(200011)65:3<243::AID-AJH12>3.0.CO;2-6
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- Article
Improved high sensitivity screen for Huntington disease using a one-step triplet-primed PCR and melting curve assay.
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- PLoS ONE, 2017, v. 12, n. 7, p. 1, doi. 10.1371/journal.pone.0180984
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- Article
Novel germline BRCA1 mutations detected in women in singapore who developed breast carcinoma before the age of 36 years.
- Published in:
- 2000
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- Publication type:
- journal article
Single-tube nonaplex microsatellite PCR panel for preimplantation genetic diagnosis of Hb Bart's hydrops fetalis syndrome.
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- Prenatal Diagnosis, 2015, v. 35, n. 6, p. 534, doi. 10.1002/pd.4568
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- Article
Rapid prenatal diagnosis of common beta-thalassemia mutations in Southeast Asia using pyrosequencing.
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- Prenatal Diagnosis, 2013, v. 33, n. 11, p. 1017, doi. 10.1002/pd.4183
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- Article
Machine learning unveils an immune-related DNA methylation profile in germline DNA from breast cancer patients.
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- Clinical Epigenetics, 2024, v. 16, n. 1, p. 1, doi. 10.1186/s13148-024-01674-2
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- Article
Loss of c- met protooncogene in primary and metastatic sites of breast cancer.
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- Annals of Surgical Oncology: An Oncology Journal for Surgeons, 1997, v. 4, n. 6, p. 499, doi. 10.1007/BF02303675
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- Article
Validation of a reverse-hybridization StripAssay for the simultaneous analysis of common α-thalassemia point mutations and deletions.
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- Clinical Chemistry & Laboratory Medicine, 2007, v. 45, n. 5, p. 605, doi. 10.1515/CCLM.2007.125
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- Publication type:
- Article
Systematic Study on Genetic and Epimutational Profile of a Cohort of Amsterdam Criteria-Defined Lynch Syndrome in Singapore.
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- PLoS ONE, 2014, v. 9, n. 4, p. 1, doi. 10.1371/journal.pone.0094170
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- Article
Enhanced Detection and Sizing of the HTT CAG Repeat Expansion in Huntington Disease Using an Improved Triplet-Primed PCR Assay.
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- Neurodegenerative Diseases, 2016, v. 16, n. 5/6, p. 348, doi. 10.1159/000444714
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- Article
Accurate Fetal Chromosome Dosage Determination by Shotgun Sequencing of Maternal Plasma DNA without PCR Amplification during Library Preparation.
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- Clinical Chemistry, 2014, v. 60, n. 4, p. 690, doi. 10.1373/clinchem.2013.216838
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- Publication type:
- Article
Methylation-Specific Triplet-Primed PCR and Melting Curve Analysis as a Rapid Screening Tool for Identifying Actionable FMR1 Genotypes.
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- Clinical Chemistry, 2013, v. 59, n. 11, p. 1668, doi. 10.1373/clinchem.2013.206771
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- Publication type:
- Article
Screening for CGG Repeat Expansion in the FMR1 Gene by Melting Curve Analysis of Combined 5' and 3' Direct Triplet-Primed PCRs.
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- Clinical Chemistry, 2012, v. 58, n. 3, p. 568, doi. 10.1373/clinchem.2011.174615
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- Publication type:
- Article