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MicroRNA-183 suppresses cancer stem-like cell properties in EBV-associated nasopharyngeal carcinoma.
- Published in:
- 2016
- By:
- Publication type:
- journal article
Disseminated peritoneal leiomyomatosis after laparoscopic supracervical hysterectomy with characteristic molecular cytogenetic findings of uterine leiomyoma.
- Published in:
- Genes, Chromosomes & Cancer, 2010, v. 49, n. 12, p. 1152, doi. 10.1002/gcc.20824
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- Publication type:
- Article
Urinary incontinence should be added to the manifestation in women with Marfan syndrome.
- Published in:
- International Urogynecology Journal, 2010, v. 21, n. 5, p. 583, doi. 10.1007/s00192-009-1078-4
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- Publication type:
- Article
Transdifferentiation of periodontal ligament-derived stem cells into retinal ganglion-like cells and its microRNA signature.
- Published in:
- Scientific Reports, 2015, p. 16429, doi. 10.1038/srep16429
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- Publication type:
- Article
Treatment Outcomes of Cesarean Scar Pregnancy Under a Novel Classification System: A Retrospective Cohort Study.
- Published in:
- Journal of Ultrasound in Medicine, 2024, v. 43, n. 8, p. 1421, doi. 10.1002/jum.16464
- By:
- Publication type:
- Article
Aberrant miR-145-5p/β-catenin signal impairs osteocyte function in adolescent idiopathic scoliosis.
- Published in:
- FASEB Journal, 2018, v. 32, n. 12, p. 6537, doi. 10.1096/fj.201800281
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- Publication type:
- Article
A pilot investigation of low-pass genome sequencing identifying site-specific variation in chromosomal mosaicisms by a multiple site sampling approach in first-trimester miscarriages.
- Published in:
- Human Reproduction, 2023, v. 38, n. 8, p. 1628, doi. 10.1093/humrep/dead090
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- Publication type:
- Article
TEDD: a database of temporal gene expression patterns during multiple developmental periods in human and model organisms.
- Published in:
- Nucleic Acids Research, 2023, v. 51, n. D1, p. D1168, doi. 10.1093/nar/gkac978
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- Publication type:
- Article
Identification of a PTEN mutation with reduced protein stability, phosphatase activity, and nuclear localization in Hong Kong patients with autistic features, neurodevelopmental delays, and macrocephaly.
- Published in:
- Autism Research: Official Journal of the International Society for Autism Research, 2018, v. 11, n. 8, p. 1098, doi. 10.1002/aur.1950
- By:
- Publication type:
- Article
Renal and extra‐renal phenotypes in a fetus with a de novo pathogenic variant in the HNF1B gene.
- Published in:
- Prenatal Diagnosis, 2024, v. 44, n. 2, p. 251, doi. 10.1002/pd.6501
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- Publication type:
- Article
Prenatal diagnosis of polycystic kidney caused by biallelic hypomorphic variants in the PKD1 gene.
- Published in:
- Prenatal Diagnosis, 2024, v. 44, n. 2, p. 247, doi. 10.1002/pd.6419
- By:
- Publication type:
- Article
Noninvasive prenatal sequencing for multiple Mendelian monogenic disorders among fetuses with skeletal dysplasia or increased nuchal translucency.
- Published in:
- Prenatal Diagnosis, 2020, v. 40, n. 11, p. 1459, doi. 10.1002/pd.5792
- By:
- Publication type:
- Article
The utility of genome-wide cell-free DNA screening in the prenatal diagnosis of Pallister-Killian syndrome.
- Published in:
- 2020
- By:
- Publication type:
- journal article
Prenatal detection of 10q22q23 duplications: dilemmas in phenotype prediction.
- Published in:
- 2016
- By:
- Publication type:
- journal article
Prevalence of recurrent pathogenic microdeletions and microduplications in over 9500 pregnancies.
- Published in:
- Prenatal Diagnosis, 2015, v. 35, n. 8, p. 801, doi. 10.1002/pd.4613
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- Publication type:
- Article
Prenatal diagnosis of 24 cases of microduplication 22q11.2: an investigation of phenotype-genotype correlations.
- Published in:
- Prenatal Diagnosis, 2015, v. 35, n. 1, p. 35, doi. 10.1002/pd.4478
- By:
- Publication type:
- Article
Recurrent structural malformations identified among Mowat-Wilson syndrome fetuses.
- Published in:
- Prenatal Diagnosis, 2014, v. 34, n. 3, p. 296, doi. 10.1002/pd.4292
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- Publication type:
- Article
Secondary findings from non-invasive prenatal testing for common fetal aneuploidies by whole genome sequencing as a clinical service.
- Published in:
- Prenatal Diagnosis, 2013, v. 33, n. 6, p. 602, doi. 10.1002/pd.4076
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- Publication type:
- Article
The detection of mosaicism by prenatal BoBs™.
- Published in:
- Prenatal Diagnosis, 2013, v. 33, n. 1, p. 42, doi. 10.1002/pd.4006
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- Publication type:
- Article
Chinese women's preferences for prenatal diagnostic procedure and their willingness to trade between procedures.
- Published in:
- Prenatal Diagnosis, 2009, v. 29, n. 13, p. 1270, doi. 10.1002/pd.2394
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- Publication type:
- Article
Chromosome Copy Number Variants in Fetuses with Syndromic Malformations.
- Published in:
- Birth Defects Research, 2017, v. 109, n. 10, p. 725, doi. 10.1002/bdr2.1054
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- Publication type:
- Article
Low-Pass Genome Sequencing-Based Detection of Paternity: Validation in Clinical Cytogenetics.
- Published in:
- Genes, 2023, v. 14, n. 7, p. 1357, doi. 10.3390/genes14071357
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- Publication type:
- Article
Diagnostic Yield of Exome Sequencing in Fetuses with Sonographic Features of Skeletal Dysplasias but Normal Karyotype or Chromosomal Microarray Analysis: A Systematic Review.
- Published in:
- Genes, 2023, v. 14, n. 6, p. 1203, doi. 10.3390/genes14061203
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- Publication type:
- Article
Implementation of Public Funded Genome Sequencing in Evaluation of Fetal Structural Anomalies.
- Published in:
- Genes, 2022, v. 13, n. 11, p. 2088, doi. 10.3390/genes13112088
- By:
- Publication type:
- Article
Clinical Implementation of Expanded Carrier Screening in Pregnant Women at Early Gestational Weeks: A Chinese Cohort Study.
- Published in:
- Genes, 2021, v. 12, n. 4, p. 496, doi. 10.3390/genes12040496
- By:
- Publication type:
- Article
First Case Report of Maternal Mosaic Tetrasomy 9p Incidentally Detected on Non-Invasive Prenatal Testing.
- Published in:
- Genes, 2021, v. 12, n. 3, p. 370, doi. 10.3390/genes12030370
- By:
- Publication type:
- Article
Clinical Significance of Non-Invasive Prenatal Screening for Trisomy 7: Cohort Study and Literature Review.
- Published in:
- Genes, 2021, v. 12, n. 1, p. 11, doi. 10.3390/genes12010011
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- Publication type:
- Article
The Pregnancy Outcome of Mosaic Embryo Transfer: A Prospective Multicenter Study and Meta-Analysis.
- Published in:
- Genes, 2020, v. 11, n. 9, p. 973, doi. 10.3390/genes11090973
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- Publication type:
- Article
A rabbit model of age-dependant ocular hypertensive response to topical corticosteroids.
- Published in:
- Acta Ophthalmologica (1755375X), 2012, v. 90, n. 6, p. 559, doi. 10.1111/j.1755-3768.2010.02016.x
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- Publication type:
- Article
A prospective study of non-invasive preimplantation genetic testing for aneuploidies (NiPGT-A) using next-generation sequencing (NGS) on spent culture media (SCM).
- Published in:
- Journal of Assisted Reproduction & Genetics, 2019, v. 36, n. 8, p. 1609, doi. 10.1007/s10815-019-01517-7
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- Publication type:
- Article
Practical Considerations in Providing Preimplantation Genetic Testing for Aneuploidies (PGT-A).
- Published in:
- Fertility & Reproduction: The Official Journal of the Asia Pacific Initiative on Reproduction (ASPIRE), 2019, v. 1, n. 1, p. 21, doi. 10.1142/S2661318219300046
- By:
- Publication type:
- Article
Trio-Based Low-Pass Genome Sequencing Reveals Characteristics and Significance of Rare Copy Number Variants in Prenatal Diagnosis.
- Published in:
- Frontiers in Genetics, 2021, v. 12, p. 1, doi. 10.3389/fgene.2021.742325
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- Publication type:
- Article
Prenatal Diagnosis and Pregnancy Outcomes of Fetuses With Orofacial Cleft: A Retrospective Cohort Study in Two Centres in Hong Kong.
- Published in:
- Cleft Palate Craniofacial Journal, 2024, v. 61, n. 3, p. 391, doi. 10.1177/10556656221128436
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- Publication type:
- Article
Genetic screening in patients with ovarian dysfunction.
- Published in:
- Clinical Genetics, 2023, v. 103, n. 3, p. 352, doi. 10.1111/cge.14267
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- Publication type:
- Article
Exome Sequencing Identifies a Novel Frameshift Mutation of MYO6 as the Cause of Autosomal Dominant Nonsyndromic Hearing Loss in a Chinese Family.
- Published in:
- Annals of Human Genetics, 2014, v. 78, n. 6, p. 410, doi. 10.1111/ahg.12084
- By:
- Publication type:
- Article
Genome-Wide Cell-Free DNA Test for Fetal Chromosomal Abnormalities and Variants: Unrestricted Versus Restricted Reporting.
- Published in:
- Diagnostics (2075-4418), 2022, v. 12, n. 10, p. 2439, doi. 10.3390/diagnostics12102439
- By:
- Publication type:
- Article
A Fetus with Congenital Microcephaly, Microphthalmia and Cataract Was Detected with Biallelic Variants in the OCLN Gene: A Case Report.
- Published in:
- Diagnostics (2075-4418), 2021, v. 11, n. 9, p. 1576, doi. 10.3390/diagnostics11091576
- By:
- Publication type:
- Article
PSCC: Sensitive and Reliable Population-Scale Copy Number Variation Detection Method Based on Low Coverage Sequencing.
- Published in:
- PLoS ONE, 2014, v. 9, n. 1, p. 1, doi. 10.1371/journal.pone.0085096
- By:
- Publication type:
- Article
CD44+ Cancer Stem-Like Cells in EBV-Associated Nasopharyngeal Carcinoma.
- Published in:
- PLoS ONE, 2012, v. 7, n. 12, p. 1, doi. 10.1371/journal.pone.0052426
- By:
- Publication type:
- Article
Prenatal Detection of Aneuploidy and Imbalanced Chromosomal Arrangements by Massively Parallel Sequencing.
- Published in:
- PLoS ONE, 2012, v. 7, n. 2, p. 1, doi. 10.1371/journal.pone.0027835
- By:
- Publication type:
- Article
MicroRNA-145 Regulates Human Corneal Epithelial Differentiation.
- Published in:
- PLoS ONE, 2011, v. 6, n. 6, p. 1, doi. 10.1371/journal.pone.0021249
- By:
- Publication type:
- Article
The CCCTC‐binding factor (CTCF)–forkhead box protein M1 axis regulates tumour growth and metastasis in hepatocellular carcinoma.
- Published in:
- Journal of Pathology, 2017, v. 243, p. 418, doi. 10.1002/path.4976
- By:
- Publication type:
- Article
The CCCTC-binding factor (CTCF)-forkhead box protein M1 axis regulates tumour growth and metastasis in hepatocellular carcinoma.
- Published in:
- Journal of Pathology, 2017, v. 243, n. 4, p. 418, doi. 10.1002/path.4976
- By:
- Publication type:
- Article
Constitutive activation of distinct NF-κB signals in EBV-associated nasopharyngeal carcinoma.
- Published in:
- Journal of Pathology, 2013, v. 231, n. 3, p. 311, doi. 10.1002/path.4239
- By:
- Publication type:
- Article
Inhibition of NOTCH3 signalling significantly enhances sensitivity to cisplatin in EBV-associated nasopharyngeal carcinoma.
- Published in:
- Journal of Pathology, 2012, v. 226, n. 3, p. 471, doi. 10.1002/path.2997
- By:
- Publication type:
- Article
Reduced CRYL1 expression in hepatocellular carcinoma confers cell growth advantages and correlates with adverse patient prognosis.
- Published in:
- Journal of Pathology, 2010, v. 220, n. 3, p. 348, doi. 10.1002/path.2644
- By:
- Publication type:
- Article
Identification of a novel 12p13.3 amplicon in nasopharyngeal carcinoma.
- Published in:
- Journal of Pathology, 2010, v. 220, n. 1, p. 97, doi. 10.1002/path.2609
- By:
- Publication type:
- Article
Effect of assisted reproductive technology on fetal brain development assessed by prenatal ultrasonography.
- Published in:
- Journal of Perinatal Medicine, 2015, v. 43, n. 1, p. 103, doi. 10.1515/jpm-2014-0020
- By:
- Publication type:
- Article
The Burden and Benefits of Knowledge: Ethical Considerations Surrounding Population-Based Newborn Genome Screening for Hearing.
- Published in:
- International Journal of Neonatal Screening (IJNS), 2022, v. 8, n. 2, p. 36, doi. 10.3390/ijns8020036
- By:
- Publication type:
- Article
Dyslexia-related loci are significantly associated with language and literacy in Chinese–English bilingual Hong Kong Chinese twins.
- Published in:
- Human Genetics, 2023, v. 142, n. 10, p. 1519, doi. 10.1007/s00439-023-02594-6
- By:
- Publication type:
- Article