Evaluation of targeted next-generation sequencing-based preimplantation genetic diagnosis of monogenic disease.
about
Pre-implantation genetic testing in ART: who will benefit and what is the evidence?Single-cell paired-end genome sequencing reveals structural variation per cell cycle.Current status of comprehensive chromosome screening for elective single-embryo transfer.Clinical utilisation of a rapid low-pass whole genome sequencing technique for the diagnosis of aneuploidy in human embryos prior to implantationSingle cell segmental aneuploidy detection is compromised by S phaseImproved sensitivity to detect recombination using qPCR for Dyskeratosis Congenita PGD.Single-cell transcriptomics: an emerging tool in the study of cardiometabolic diseaseHigh-throughput carrier screening using TaqMan allelic discrimination.A healthy delivery of twins by assisted reproduction followed by preimplantation genetic screening in a woman with X-linked dominant incontinentia pigmenti.Clinical outcome of preimplantation genetic diagnosis and screening using next generation sequencing.Mutation spectrum of six genes in Chinese phenylketonuria patients obtained through next-generation sequencing.Detection and phasing of single base de novo mutations in biopsies from human in vitro fertilized embryos by advanced whole-genome sequencingGenetic considerations in recurrent pregnancy loss.Application of next-generation sequencing technology for comprehensive aneuploidy screening of blastocysts in clinical preimplantation genetic screening cycles.Preimplantation Genetic Diagnosis: Prenatal Testing for Embryos Finally Achieving Its PotentialRandomized comparison of next-generation sequencing and array comparative genomic hybridization for preimplantation genetic screening: a pilot studyManagement of Incidental Findings in the Era of Next-generation SequencingApplication of next-generation sequencing for 24-chromosome aneuploidy screening of human preimplantation embryosClinical Considerations of Preimplantation Genetic Diagnosis for Monogenic Diseases.Can Comprehensive Chromosome Screening Technology Improve IVF/ICSI Outcomes? A Meta-AnalysisHealthy Baby Born to a Robertsonian Translocation Carrier following Next-Generation Sequencing-Based Preimplantation Genetic Diagnosis: A Case Report.Live births after simultaneous avoidance of monogenic diseases and chromosome abnormality by next-generation sequencing with linkage analysesAneuploidy analysis in day 7 human blastocysts produced by in vitro fertilization.DNA sequencing methods in human genetics and disease research.Preimplantation genetic diagnosis guided by single-cell genomics.Comparative study of single-nucleotide polymorphism array and next generation sequencing based strategies on triploid identification in preimplantation genetic diagnosis and screen.Advances in preimplantation genetic diagnosis/screening.Diagnosis of human preimplantation embryo viability.Concise Review: Patient-Derived Stem Cell Research for Monogenic Disorders.How should we choose the 'best' embryo? A commentary on behalf of the British Fertility Society and the Association of Clinical Embryologists.Gestational surrogacy and the role of routine embryo screening: Current challenges and future directions for preimplantation genetic testing.Implementing PGD/PGD-A in IVF clinics: considerations for the best laboratory approach and management.Preimplantation genetic testing for aneuploidy: what technology should you use and what are the differences?Next-generation molecular diagnosis: single-cell sequencing from bench to bedside.Karyomapping and how is it improving preimplantation genetics?Preimplantation genetic haplotyping for six Chinese pedigrees with thalassemia using a single nucleotide polymorphism microarray.Reanalysis of human blastocysts with different molecular genetic screening platforms reveals significant discordance in ploidy statusPreimplantation genetic diagnosis for inherited neurological disorders.Preimplantation genetic diagnosis: an update on current technologies and ethical considerations.Preclinical validation of a targeted next generation sequencing-based comprehensive chromosome screening methodology in human blastocysts.
P2860
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P2860
Evaluation of targeted next-generation sequencing-based preimplantation genetic diagnosis of monogenic disease.
description
2013 nî lūn-bûn
@nan
2013年の論文
@ja
2013年学术文章
@wuu
2013年学术文章
@zh
2013年学术文章
@zh-cn
2013年学术文章
@zh-hans
2013年学术文章
@zh-my
2013年学术文章
@zh-sg
2013年學術文章
@yue
2013年學術文章
@zh-hant
name
Evaluation of targeted next-ge ...... iagnosis of monogenic disease.
@en
Evaluation of targeted next-ge ...... iagnosis of monogenic disease.
@nl
type
label
Evaluation of targeted next-ge ...... iagnosis of monogenic disease.
@en
Evaluation of targeted next-ge ...... iagnosis of monogenic disease.
@nl
prefLabel
Evaluation of targeted next-ge ...... iagnosis of monogenic disease.
@en
Evaluation of targeted next-ge ...... iagnosis of monogenic disease.
@nl
P2093
P1476
Evaluation of targeted next-ge ...... iagnosis of monogenic disease.
@en
P2093
Anastasia Fedick
Batsal Devkota
Nathan R Treff
Richard T Scott
P304
1377-1384.e6
P356
10.1016/J.FERTNSTERT.2012.12.018
P407
P577
2013-01-09T00:00:00Z