Found: 19
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Trio-Based Low-Pass Genome Sequencing Reveals Characteristics and Significance of Rare Copy Number Variants in Prenatal Diagnosis.
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- Frontiers in Genetics, 2021, v. 12, p. 1, doi. 10.3389/fgene.2021.742325
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- Article
Cell‐free DNA test for fetal chromosomal abnormalities in multiple pregnancies.
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- Acta Obstetricia et Gynecologica Scandinavica, 2024, v. 103, n. 9, p. 1799, doi. 10.1111/aogs.14901
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- Article
The role of chromosomal microarray analysis among fetuses with normal karyotype and single system anomaly or nonspecific sonographic findings.
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- Acta Obstetricia et Gynecologica Scandinavica, 2021, v. 100, n. 2, p. 235, doi. 10.1111/aogs.14003
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- Article
Amniotic fluid gamma-glutamyl transferase for prediction of biliary atresia in cases of non-visualisation of the fetal gallbladder: a retrospective study using a validated analytical platform and local reference range.
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- Hong Kong Medical Journal, 2024, v. 30, n. 3, p. 218, doi. 10.12809/hkmj2210567
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- Article
Homology-independent multiallelic disruption via CRISPR/Cas9-based knock-in yields distinct functional outcomes in human cells.
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- BMC Biology, 2018, v. 16, n. 1, p. 1, doi. 10.1186/s12915-018-0616-2
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- Article
Mate-pair genome sequencing reveals structural variants for idiopathic male infertility.
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- Human Genetics, 2023, v. 142, n. 3, p. 363, doi. 10.1007/s00439-022-02510-4
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- Article
Deciphering the complexity of simple chromosomal insertions by genome sequencing.
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- Human Genetics, 2021, v. 140, n. 2, p. 361, doi. 10.1007/s00439-020-02210-x
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- Article
Low-pass genome sequencing: a validated method in clinical cytogenetics.
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- Human Genetics, 2020, v. 139, n. 11, p. 1403, doi. 10.1007/s00439-020-02185-9
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- Article
Embryonic and fetal globins are expressed in adult erythroid progenitor cells and in erythroid cell cultures.
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- Prenatal Diagnosis, 2001, v. 21, n. 7, p. 529, doi. 10.1002/pd.81
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- Article
Prenatal Diagnosis of Fetuses With Increased Nuchal Translucency by Genome Sequencing Analysis.
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- Frontiers in Genetics, 2019, p. 1, doi. 10.3389/fgene.2019.00761
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- Article
A prospective study of non-invasive preimplantation genetic testing for aneuploidies (NiPGT-A) using next-generation sequencing (NGS) on spent culture media (SCM).
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- Journal of Assisted Reproduction & Genetics, 2019, v. 36, n. 8, p. 1609, doi. 10.1007/s10815-019-01517-7
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- Article
Practical Considerations in Providing Preimplantation Genetic Testing for Aneuploidies (PGT-A).
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- 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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- Article
Genome-Wide Cell-Free DNA Test for Fetal Chromosomal Abnormalities and Variants: Unrestricted Versus Restricted Reporting.
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- Diagnostics (2075-4418), 2022, v. 12, n. 10, p. 2439, doi. 10.3390/diagnostics12102439
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- Article
TEDD: a database of temporal gene expression patterns during multiple developmental periods in human and model organisms.
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- Nucleic Acids Research, 2023, v. 51, n. D1, p. D1168, doi. 10.1093/nar/gkac978
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- Article
Maternal plasma or human serum albumin in wash buffer enhances enrichment and ex vivo expansion of human umbilical cord blood CD34<sup>+</sup> cells.
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- British Journal of Haematology, 2007, v. 137, n. 5, p. 468, doi. 10.1111/j.1365-2141.2007.06606.x
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- Article
The detection of mosaicism by prenatal BoBs™.
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- Prenatal Diagnosis, 2013, v. 33, n. 1, p. 42, doi. 10.1002/pd.4006
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- Article
Detection of the S252W mutation in fibroblast growth factor receptor 2 (FGFR2) in fetal DNA from maternal plasma in a pregnancy affected by Apert syndrome.
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- Prenatal Diagnosis, 2011, v. 31, n. 2, p. 218, doi. 10.1002/pd.2672
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- Article
Simple non-invasive prenatal detection of Hb Bart's disease by analysis of fetal erythrocytes in maternal blood.
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- Prenatal Diagnosis, 2005, v. 25, n. 2, p. 123, doi. 10.1002/pd.1096
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- Article
Low-Pass Genome Sequencing-Based Detection of Paternity: Validation in Clinical Cytogenetics.
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- Genes, 2023, v. 14, n. 7, p. 1357, doi. 10.3390/genes14071357
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- Article