135 results on '"Chan, Kelvin Yuen‐Kwong"'
Search Results
2. Comprehensive analysis of recessive carrier status using exome and genome sequencing data in 1543 Southern Chinese
3. Fetal Hyperthyroidism with Maternal Hypothyroidism: Two Cases of Intrauterine Therapy
4. Coexistence of paternally-inherited ABCC8 mutation and mosaic paternal uniparental disomy 11p hyperinsulinism
5. Cost-effectiveness analysis of chromosomal microarray as a primary test for prenatal diagnosis in Hong Kong
6. Application of Prenatal Whole Exome Sequencing for Structural Congenital Anomalies—Experience from a Local Prenatal Diagnostic Laboratory
7. Informed choice and decision making in women offered cell‐free DNA prenatal genetic screening
8. Significance of the Myxovirus Resistance A (MxA) Gene –123C>A Single-Nucleotide Polymorphism in Suppressed Interferon β Induction of Severe Acute Respiratory Syndrome Coronavirus Infection
9. The Role of Pea3 Group Transcription Factors in Esophageal Squamous Cell Carcinoma
10. Evaluating the Clinical Utility of Genome Sequencing for Cytogenetically Balanced Chromosomal Abnormalities in Prenatal Diagnosis
11. Generation of genomic-integration-free human induced pluripotent stem cells and the derived cardiomyocytes of X-linked dilated cardiomyopathy from DMD gene mutation
12. Regarding “Co-expression of SNAIL and TWIST determines prognosis in estrogen receptor-positive early breast cancer patients”
13. Prenatal and postnatal diagnosis of Schuurs‐Hoeijmakers syndrome: Case series and review of the literature
14. Prenatal diagnosis and long‐term follow‐up of a Chinese patient with mosaic variegated aneuploidy and its molecular analysis
15. A Small‐Molecule AIE Chromosome Periphery Probe for Cytogenetic Studies
16. Significance of the myxovirus resistance A (MxA) gene -123C>a single-nucleotide polymorphism in suppressed interferon (beta) induction of severe acute respiratory syndrome coronavirus infection
17. Epigenetic and genetic alterations of p33ING1b in ovarian cancer
18. Development of cytogenomics for prenatal diagnosis: from chromosomes to single nucleotides: a review
19. Decision outcomes of women choosing extended non-invasive prenatal testing
20. Exome sequencing identifies molecular diagnosis in children with drug-resistant epilepsy
21. Paternal uniparental disomy of chromosome 19 in a pair of monochorionic diamniotic twins with dysmorphic features and developmental delay
22. Prenatal and postnatal diagnosis of Schuurs‐Hoeijmakers syndrome: Case series and review of the literature.
23. Paternal uniparental disomy of chromosome 19 in a pair of monochorionic diamniotic twins with dysmorphic features and developmental delay
24. Effect of knowledge on women’s likely uptake of and willingness to pay for non-invasive test (NIPT)
25. Decision outcomes in women offered noninvasive prenatal test (NIPT) for positive Down screening results
26. Use of clinical chromosomal microarray in Chinese patients with autism spectrum disorder—implications of a copy number variation involving DPP10
27. Women’s stated test preference on questionnaire versus their actual choice in real clinical setting regarding non-invasive prenatal test
28. Study of the extent of information desired by women undergoing non-invasive prenatal testing following positive prenatal Down-syndrome screening test results
29. Exome sequencing identifies molecular diagnosis in children with drug‐resistant epilepsy.
30. Comparison of 6q25 Breast Cancer Hits from Asian and European Genome Wide Association Studies in the Breast Cancer Association Consortium (BCAC)
31. Pregnancy‐associated plasma protein A for prediction of fetal growth restriction
32. Functional polymorphisms in the promoter of BRCA1 influences transcription and are associated with decreased risk for breast cancer in Chinese women
33. Decision outcomes in women offered noninvasive prenatal test (NIPT) for positive Down screening results.
34. Genome-Wide Association Study of Hepatocellular Carcinoma in Southern Chinese Patients with Chronic Hepatitis B Virus Infection
35. Regarding “Co-expression of SNAIL and TWIST determines prognosis in estrogen receptor-positive early breast cancer patients”
36. Prevalence and Risk Factors of Human Papillomavirus (HPV) Infection in Southern Chinese Women – A Population-Based Study
37. CD209 (DC-SIGN) −336A>G promoter polymorphism and severe acute respiratory syndrome in Hong Kong Chinese
38. Significance of the Myxovirus Resistance A (MxA) Gene −123C>A Single‐Nucleotide Polymorphism in Suppressed Interferon β Induction of Severe Acute Respiratory Syndrome Coronavirus Infection
39. Abstract 3156: eIF4E in human breast cancer and its role in regulating translation of splice variants of breast cancer genes
40. Abstract 2040: Identification of microRNAs associated with tamoxifen resistance in breast cancer
41. Hypermethylation of RAS effector related genes and DNA methyltransferase 1 expression in endometrial carcinogenesis
42. A novel subset of putative stem/progenitor CD34+Oct-4+ cells is the major target for SARS coronavirus in human lung
43. Expression of ΔNp73 and TAp73α Independently Associated with Radiosensitivities and Prognoses in Cervical Squamous Cell Carcinoma
44. Enhancement of the radiosensitivity of cervical cancer cells by overexpressing p73α
45. Epigenetic and genetic alterations of p33 ING1b in ovarian cancer
46. p73 Expression Is Associated with the Cellular Radiosensitivity in Cervical Cancer after Radiotherapy
47. Prognostic significance of minichromosome maintenance proteins in breast cancer
48. The limits of personalization in precision medicine: Polygenic risk scores and racial categorization in a precision breast cancer screening trial
49. Targeted sequencing of lung function loci in chronic obstructive pulmonary disease cases and controls
50. Comparative evaluation of the Minimally-Invasive Karyotyping (MINK) algorithm for non-invasive prenatal testing
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