Found: 30
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Genome-Wide Gene Expression Analysis Implicates the Immune Response and Lymphangiogenesis in the Pathogenesis of Fetal Chylothorax.
- Published in:
- PLoS ONE, 2012, v. 7, n. 4, p. 1, doi. 10.1371/journal.pone.0034901
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- Publication type:
- Article
Low-molecular-weight-heparin can benefit women with recurrent pregnancy loss and sole protein S deficiency: a historical control cohort study from Taiwan.
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- Thrombosis Journal, 2016, v. 14, p. 1, doi. 10.1186/s12959-016-0118-9
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- Publication type:
- Article
Preimplantation genetic diagnosis of hemophilia A.
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- Thrombosis Journal, 2016, v. 14, p. 79, doi. 10.1186/s12959-016-0098-9
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- Publication type:
- Article
De novo mutation and somatic mosaicism of gene mutation in type 2A, 2B and 2M VWD.
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- Thrombosis Journal, 2016, v. 14, p. 3, doi. 10.1186/s12959-016-0092-2
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- Publication type:
- Article
SMAD2 as risk locus for human left atrial isomerism detected by mother-fetus-pair exome sequencing and imaging studies.
- Published in:
- 2019
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- Publication type:
- Letter
Low-molecular-weight heparin associated with reduced fetal fraction and subsequent false-negative cell-free DNA test result for trisomy 21.
- Published in:
- 2018
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- Publication type:
- Letter
Origin and timing of de novo variants implicated in type 2 von Willebrand disease.
- Published in:
- Journal of Cellular & Molecular Medicine, 2022, v. 26, n. 21, p. 5403, doi. 10.1111/jcmm.17563
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- Publication type:
- Article
Mitochondrial phylogeny reveals the artificial introduction of the pale chub Zacco platypus (Cyprinidae) in Taiwan.
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- Ichthyological Research, 2006, v. 53, n. 4, p. 323, doi. 10.1007/s10228-006-0353-3
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- Publication type:
- Article
Noninvasive prenatal diagnosis of fetal aneuploidy by circulating fetal nucleated red blood cells and extravillous trophoblasts using silicon-based nanostructured microfluidics.
- Published in:
- Molecular Cytogenetics (17558166), 2017, v. 10, p. 1, doi. 10.1186/s13039-017-0343-3
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- Publication type:
- Article
A pilot proof-of-principle study to compare fresh and vitrified cycle preimplantation genetic screening by chromosome microarray and next generation sequencing.
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- Molecular Cytogenetics (17558166), 2016, v. 9, p. 1, doi. 10.1186/s13039-016-0238-8
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- Publication type:
- Article
Preimplantation genetic screening of blastocysts by multiplex qPCR followed by fresh embryo transfer: validation and verification.
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- Molecular Cytogenetics (17558166), 2015, v. 8, n. 1, p. 1, doi. 10.1186/s13039-015-0140-9
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- Publication type:
- Article
Skewed X-Chromosome Inactivation and Parental Gonadal Mosaicism Are Implicated in X-Linked Recessive Female Hemophilia Patients.
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- Diagnostics (2075-4418), 2022, v. 12, n. 10, p. 2267, doi. 10.3390/diagnostics12102267
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- Publication type:
- Article
Proposal for Practical Approach in Prenatal Diagnosis of Beckwith–Wiedemann Syndrome and Review of the Literature.
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- Diagnostics (2075-4418), 2022, v. 12, n. 7, p. N.PAG, doi. 10.3390/diagnostics12071709
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- Publication type:
- Article
Preimplantation Genetic Diagnosis in Hereditary Hearing Impairment.
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- Diagnostics (2075-4418), 2021, v. 11, n. 12, p. 2395, doi. 10.3390/diagnostics11122395
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- Publication type:
- Article
Prenatal Diagnosis of True Fetal Mosaicism with Small Supernumerary Marker Chromosome Derived from Chromosome 16 by Funipuncture and Molecular Cytogenetics Including Chromosome Microarray.
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- Diagnostics (2075-4418), 2021, v. 11, n. 8, p. 1457, doi. 10.3390/diagnostics11081457
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- Publication type:
- Article
Comparison of Genetic Profiling between Primary Tumor and Circulating Tumor Cells Captured by Microfluidics in Epithelial Ovarian Cancer: Tumor Heterogeneity or Allele Dropout?
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- Diagnostics (2075-4418), 2021, v. 11, n. 6, p. 1102, doi. 10.3390/diagnostics11061102
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- Publication type:
- Article
Whole Exome Sequencing with Comprehensive Gene Set Analysis Identified a Biparental-Origin Homozygous c.509G>A Mutation in PPIB Gene Clustered in Two Taiwanese Families Exhibiting Fetal Skeletal Dysplasia during Prenatal Ultrasound.
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- Diagnostics (2075-4418), 2020, v. 10, n. 5, p. 286, doi. 10.3390/diagnostics10050286
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- Publication type:
- Article
Prenatal Diagnosis of Autosomal Recessive Renal Tubular Dysgenesis with Anhydramnios Caused by a Mutation in the AGT Gene.
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- Diagnostics (2075-4418), 2019, v. 9, n. 4, p. 185, doi. 10.3390/diagnostics9040185
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- Publication type:
- Article
Preimplantation Genetic Diagnosis of Neurodegenerative Diseases: Review of Methodologies and Report of Our Experience as a Regional Reference Laboratory.
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- Diagnostics (2075-4418), 2019, v. 9, n. 2, p. 44, doi. 10.3390/diagnostics9020044
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- Publication type:
- Article
Difficulties of Prenatal Genetic Counseling for a Subsequent Child in a Family With Multiple Genetic Variations.
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- Frontiers in Genetics, 2021, v. 12, p. 1, doi. 10.3389/fgene.2021.612100
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- Publication type:
- Article
A compound heterozygous GNPTAB mutation causes mucolipidosis II with marked hair color change in a Han Chinese baby.
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- American Journal of Medical Genetics. Part A, 2011, v. 155A, n. 4, p. 931, doi. 10.1002/ajmg.a.33834
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- Publication type:
- Article
A recurrent ITGA9 missense mutation in human fetuses with severe chylothorax: possible correlation with poor response to fetal therapy.
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- Prenatal Diagnosis, 2008, v. 28, n. 11, p. 1057, doi. 10.1002/pd.2130
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- Publication type:
- Article
Proinflammatory macrophage migratory inhibition factor and interleukin-6 are concentrated in pleural effusion of human fetuses with prenatal chylothorax.
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- Prenatal Diagnosis, 2007, v. 27, n. 5, p. 435, doi. 10.1002/pd.1704
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- Publication type:
- Article
A Silicon-based Coral-like Nanostructured Microfluidics to Isolate Rare Cells in Human Circulation: Validation by SK-BR-3 Cancer Cell Line and Its Utility in Circulating Fetal Nucleated Red Blood Cells.
- Published in:
- Micromachines, 2019, v. 10, n. 2, p. 132, doi. 10.3390/mi10020132
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- Publication type:
- Article
Relevance of Copy Number Variation at Chromosome X in Male Fetuses Inherited from the Mother May Be Ascertained by Including Male Relatives from the Maternal Lineage in Addition to Trio Analyses.
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- Genes, 2020, v. 11, n. 9, p. 979, doi. 10.3390/genes11090979
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- Publication type:
- Article
Species and sex comparisons of karyotype and genome size in two Kurixalus tree frogs (Anura, Rhacophoridae).
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- Acta Herpetologica, 2017, v. 12, n. 2, p. 139, doi. 10.13128/Acta_Herpetol-20742
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- Publication type:
- Article
De Novo Noninversion Variants Implicated in Sporadic Hemophilia A: A Variant Origin and Timing Study.
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- International Journal of Molecular Sciences, 2024, v. 25, n. 3, p. 1763, doi. 10.3390/ijms25031763
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- Publication type:
- Article
Fosmid library end sequencing reveals a rarely known genome structure of marine shrimp Penaeus monodon.
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- BMC Genomics, 2011, v. 12, n. 1, p. 242, doi. 10.1186/1471-2164-12-242
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- Publication type:
- Article
AFLPs congruent with morphological differentiation of Asian common minnow Zacco (Pisces: Cyprinidae) in Taiwan.
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- Zoologica Scripta, 2006, v. 35, n. 4, p. 341, doi. 10.1111/j.1463-6409.2006.00232.x
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- Publication type:
- Article
Genome-Wide Microarray Analysis Suggests Transcriptomic Response May Not Play a Major Role in High- to Low-Altitude Acclimation in Harvest Mouse (Micromys minutus).
- Published in:
- Animals (2076-2615), 2019, v. 9, n. 3, p. 92, doi. 10.3390/ani9030092
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- Publication type:
- Article