Found: 16
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Study of the extent of information desired by women undergoing non-invasive prenatal testing following positive prenatal Down-syndrome screening test results.
- Published in:
- 2017
- By:
- Publication type:
- journal article
A Small‐Molecule AIE Chromosome Periphery Probe for Cytogenetic Studies.
- Published in:
- Angewandte Chemie, 2020, v. 132, n. 26, p. 10413, doi. 10.1002/ange.201916718
- By:
- Publication type:
- Article
Evaluating the Clinical Utility of Genome Sequencing for Cytogenetically Balanced Chromosomal Abnormalities in Prenatal Diagnosis.
- Published in:
- Frontiers in Genetics, 2021, v. 11, p. N.PAG, doi. 10.3389/fgene.2020.620162
- By:
- Publication type:
- Article
Prenatal and postnatal diagnosis of Schuurs‐Hoeijmakers syndrome: Case series and review of the literature.
- Published in:
- American Journal of Medical Genetics. Part A, 2021, v. 185, n. 2, p. 384, doi. 10.1002/ajmg.a.61964
- By:
- Publication type:
- Article
Cost-effectiveness analysis of chromosomal microarray as a primary test for prenatal diagnosis in Hong Kong.
- Published in:
- 2020
- By:
- Publication type:
- journal article
Pregnancy-associated plasma protein A for prediction of fetal growth restriction.
- Published in:
- International Journal of Gynecology & Obstetrics, 2015, v. 130, n. 2, p. 200, doi. 10.1016/j.ijgo.2015.02.016
- By:
- Publication type:
- Article
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.
- Published in:
- 2010
- By:
- Publication type:
- journal article
Comprehensive analysis of recessive carrier status using exome and genome sequencing data in 1543 Southern Chinese.
- Published in:
- NPJ Genomic Medicine, 2022, v. 7, n. 1, p. 1, doi. 10.1038/s41525-022-00287-z
- By:
- Publication type:
- Article
Application of Prenatal Whole Exome Sequencing for Structural Congenital Anomalies—Experience from a Local Prenatal Diagnostic Laboratory.
- Published in:
- Healthcare (2227-9032), 2022, v. 10, n. 12, p. 2521, doi. 10.3390/healthcare10122521
- By:
- Publication type:
- Article
Exome sequencing identifies molecular diagnosis in children with drug‐resistant epilepsy.
- Published in:
- Epilepsia Open, 2019, v. 4, n. 1, p. 63, doi. 10.1002/epi4.12282
- By:
- Publication type:
- Article
Prenatal diagnosis and long‐term follow‐up of a Chinese patient with mosaic variegated aneuploidy and its molecular analysis.
- Published in:
- Clinical Case Reports, 2020, v. 8, n. 8, p. 1369, doi. 10.1002/ccr3.2802
- By:
- Publication type:
- Article
Hypermethylation of RAS effector related genes and DNA methyltransferase 1 expression in endometrial carcinogenesis.
- Published in:
- International Journal of Cancer, 2008, v. 123, n. 2, p. 296, doi. 10.1002/ijc.23494
- By:
- Publication type:
- Article
A Small‐Molecule AIE Chromosome Periphery Probe for Cytogenetic Studies.
- Published in:
- Angewandte Chemie International Edition, 2020, v. 59, n. 26, p. 10327, doi. 10.1002/anie.201916718
- By:
- Publication type:
- Article
Fetal Hyperthyroidism with Maternal Hypothyroidism: Two Cases of Intrauterine Therapy.
- Published in:
- 2024
- By:
- Publication type:
- Case Study
Informed choice and decision making in women offered cell-free DNA prenatal genetic screening.
- Published in:
- 2017
- By:
- Publication type:
- Letter
Coexistence of paternally-inherited ABCC8 mutation and mosaic paternal uniparental disomy 11p hyperinsulinism.
- Published in:
- International Journal of Pediatric Endocrinology, 2020, v. 2020, n. 1, p. 1, doi. 10.1186/s13633-020-00083-5
- By:
- Publication type:
- Article