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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
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
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- Publication type:
- Article
Prenatal Diagnosis of Fetuses With Increased Nuchal Translucency by Genome Sequencing Analysis.
- Published in:
- Frontiers in Genetics, 2019, p. 1, doi. 10.3389/fgene.2019.00761
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- Publication type:
- Article
Histological and microRNA Signatures of Corneal Epithelium in Keratoconus.
- Published in:
- Journal of Refractive Surgery, 2018, v. 34, n. 3, p. 201, doi. 10.3928/1081597X-20171215-02
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- 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
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- Publication type:
- Article
Mate-pair genome sequencing reveals structural variants for idiopathic male infertility.
- Published in:
- Human Genetics, 2023, v. 142, n. 3, p. 363, doi. 10.1007/s00439-022-02510-4
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- Publication type:
- Article
Deciphering the complexity of simple chromosomal insertions by genome sequencing.
- Published in:
- Human Genetics, 2021, v. 140, n. 2, p. 361, doi. 10.1007/s00439-020-02210-x
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- Publication type:
- Article
Low-pass genome sequencing: a validated method in clinical cytogenetics.
- Published in:
- Human Genetics, 2020, v. 139, n. 11, p. 1403, doi. 10.1007/s00439-020-02185-9
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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
Glucose-6-phosphatase gene (727G→T) splicing mutation is prevalent in Hong Kong Chinese patients with glycogen storage disease type la.
- Published in:
- Clinical Genetics, 1998, v. 53, n. 3, p. 184, doi. 10.1111/j.1399-0004.1998.tb02674.x
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- Publication type:
- Article
Autism‐associated PTEN missense mutation leads to enhanced nuclear localization and neurite outgrowth in an induced pluripotent stem cell line.
- Published in:
- FEBS Journal, 2020, v. 287, n. 22, p. 4848, doi. 10.1111/febs.15287
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- 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
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- 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
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- 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
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
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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
Investigation of Chromosomal Structural Abnormalities in Patients With Undiagnosed Neurodevelopmental Disorders.
- Published in:
- Frontiers in Genetics, 2022, v. 13, p. 1, doi. 10.3389/fgene.2022.803088
- 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
- By:
- 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
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
- By:
- 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
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- Publication type:
- Article
Case Report: Prenatal Recurrent Microcephaly and Corpus Callosum Abnormalities in a Chinese Family with Novel Biallelic SASS6 Mutations.
- Published in:
- Fetal Diagnosis & Therapy, 2023, v. 50, n. 2, p. 84, doi. 10.1159/000529504
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- Publication type:
- Article
Tyrosinase gene ( TYR) mutations in Chinese patients with oculocutaneous albinism type 1.
- Published in:
- Clinical & Experimental Ophthalmology, 2010, v. 38, n. 1, p. 37, doi. 10.1111/j.1442-9071.2009.02220.x
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- Publication type:
- Article
Two cases of X-linked juvenile retinoschisis with different optical coherence tomography findings and RS1 gene mutations.
- Published in:
- Clinical & Experimental Ophthalmology, 2004, v. 32, n. 4, p. 429, doi. 10.1111/j.1442-9071.2004.00820.x
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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
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
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- 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
- By:
- 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
Sonogenetics: A Breakthrough in Prenatal Diagnosis.
- Published in:
- Donald School Journal of Ultrasound in Obstetrics & Gynecology, 2011, v. 5, n. 1, p. 73
- By:
- 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
MicroRNA‐132 directs human periodontal ligament‐derived neural crest stem cell neural differentiation.
- Published in:
- Journal of Tissue Engineering & Regenerative Medicine, 2019, v. 13, n. 1, p. 12, doi. 10.1002/term.2759
- 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
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- 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
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
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- Publication type:
- Article
Identification of cryptic balanced translocations in couples with unexplained recurrent pregnancy loss based upon embryonic PGT-A results.
- Published in:
- Journal of Assisted Reproduction & Genetics, 2024, v. 41, n. 1, p. 171, doi. 10.1007/s10815-023-02999-2
- By:
- 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
- By:
- Publication type:
- Article
Prevalence of mutations in the BRCA1 gene among Chinese patients with breast cancer.
- Published in:
- 1999
- By:
- Publication type:
- journal article
Neuropathological signatures revealed by transcriptomic and proteomic analysis in Pten-deficient mouse models.
- Published in:
- Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-33869-7
- By:
- Publication type:
- Article