about
PGS-FISH in reproductive medicine and perspective directions for improvement: a systematic reviewWhole-genome sequencing in health care. Recommendations of the European Society of Human Genetics.ESHRE PGD Consortium data collection XII: cycles from January to December 2009 with pregnancy follow-up to October 2010.Outcomes of in vitro fertilization with preimplantation genetic diagnosis: an analysis of the United States Assisted Reproductive Technology Surveillance Data, 2011-2012Transferring embryos with indeterminate PGD results: the ethical implications.ESHRE PGD Consortium data collection X: cycles from January to December 2007 with pregnancy follow-up to October 2008.Improved sensitivity to detect recombination using qPCR for Dyskeratosis Congenita PGD.The ESHRE PGD Consortium: 10 years of data collection.Preimplantation genetic diagnosis: state of the art 2011.ESHRE PGD Consortium data collection XI: cycles from January to December 2008 with pregnancy follow-up to October 2009.Singling out genetic disorders and disease.Clinical outcome of preimplantation genetic diagnosis and screening using next generation sequencing.Evaluation of PCR-based preimplantation genetic diagnosis applied to monogenic diseases: a collaborative ESHRE PGD consortium study.Pregnancy after PGD for recessive dystrophic epidermolysis bullosa inversa: genetics and preimplantation genetics.An update of preimplantation genetic diagnosis in gene diseases, chromosomal translocation, and aneuploidy screeningPreimplantation genetic diagnosis (PGD) for Huntington's disease: the experience of three European centresLive births after simultaneous avoidance of monogenic diseases and chromosome abnormality by next-generation sequencing with linkage analysesFalse positive rate of an arrayCGH platform for single-cell preimplantation genetic screening and subsequent clinical application on day-3The experience of 3 years of external quality assessment of preimplantation genetic diagnosis for cystic fibrosisDiscrepant diagnosis rate of array comparative genomic hybridization in thawed euploid blastocysts.Preimplantation genetic diagnosis of P450 oxidoreductase deficiency and Huntington Disease using three different molecular approaches simultaneouslyFamilial haplotyping and embryo analysis for Preimplantation genetic diagnosis (PGD) using DNA microarrays: a proof of principle study.Accreditation of the PGD laboratory.Simple and Easy to Perform Preimplantation Genetic Diagnosis for β-thalassemia Major Using Combination of Conventional and Fluorescent Polymerase Chain Reaction.Preimplantation genetic testing: indications and controversiesA methodological overview on molecular preimplantation genetic diagnosis and screening: a genomic future?Advances in preimplantation genetic diagnosis/screening.Replication independent DNA double-strand break retention may prevent genomic instabilityHow should we choose the 'best' embryo? A commentary on behalf of the British Fertility Society and the Association of Clinical Embryologists.Single-tube nonaplex microsatellite PCR panel for preimplantation genetic diagnosis of Hb Bart's hydrops fetalis syndrome.Outcomes of medical malpractice claims in assisted reproductive technology over a 10-year period from a single carrier.Blastocyst biopsy and vitrification are effective for preimplantation genetic diagnosis of monogenic diseases.Improving preimplantation genetic diagnosis (PGD) reliability by selection of sperm donor with the most informative haplotype.The clinical application of preimplantation genetic diagnosis for the patient affected by congenital contractural arachnodactyly and spinal and bulbar muscular atrophy.The uptake and outcome of prenatal and pre-implantation genetic diagnosis for Huntington's disease in the Netherlands (1998-2008).Diagnosis of parental balanced reciprocal translocations by trophectoderm biopsy and comprehensive chromosomal screening.A generic, flexible protocol for preimplantation human leukocyte antigen typing alone or in combination with a monogenic disease, for rapid case work-up and application.PGD for reciprocal and Robertsonian translocations using array comparative genomic hybridization.Challenges, Dilemmas and Factors Involved in PGD Decision-Making: Providers' and Patients' Views, Experiences and Decisions.Sensitive Monogenic Noninvasive Prenatal Diagnosis by Targeted Haplotyping.
P2860
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P2860
description
2009 nî lūn-bûn
@nan
2009年の論文
@ja
2009年学术文章
@wuu
2009年学术文章
@zh
2009年学术文章
@zh-cn
2009年学术文章
@zh-hans
2009年学术文章
@zh-my
2009年学术文章
@zh-sg
2009年學術文章
@yue
2009年學術文章
@zh-hant
name
The causes of misdiagnosis and adverse outcomes in PGD.
@en
The causes of misdiagnosis and adverse outcomes in PGD.
@nl
type
label
The causes of misdiagnosis and adverse outcomes in PGD.
@en
The causes of misdiagnosis and adverse outcomes in PGD.
@nl
prefLabel
The causes of misdiagnosis and adverse outcomes in PGD.
@en
The causes of misdiagnosis and adverse outcomes in PGD.
@nl
P2093
P2860
P356
P1433
P1476
The causes of misdiagnosis and adverse outcomes in PGD.
@en
P2093
A Thornhill
J C Harper
J Traeger-Synodinos
K D Sermon
P2860
P304
P356
10.1093/HUMREP/DEN488
P407
P577
2009-01-20T00:00:00Z