| scholarly article | Q13442814 |
| P356 | DOI | 10.1586/17474108.3.5.635 |
| P2093 | author name string | Santiago Munné | |
| P2860 | cites work | Pregnancy and delivery of healthy infants developed from vitrified oocytes in a stimulated in vitro fertilization-embryo transfer program | Q48886538 |
| Pregnancies following pre-conception diagnosis of common aneuploidies by fluorescent in-situ hybridization | Q49047326 | ||
| Oocyte karyotyping by comparative genomic hybridization [correction of hybrydization] provides a highly reliable method for selecting "competent" embryos, markedly improving in vitro fertilization outcome: a multiphase study. | Q50639751 | ||
| Multiple micromanipulations for preimplantation genetic diagnosis do not affect embryo development to the blastocyst stage. | Q50649629 | ||
| Wide range of chromosome abnormalities in the embryos of young egg donors. | Q50651270 | ||
| The beneficial effects of preimplantation genetic diagnosis for aneuploidy support extensive clinical application. | Q50661217 | ||
| Influence of maternal age on the outcome of PGD for aneuploidy screening in patients with recurrent implantation failure. | Q50661225 | ||
| Efficacy and clinical outcome of preimplantation genetic diagnosis using FISH for couples of reciprocal and Robertsonian translocations: the Korean experience. | Q50672374 | ||
| Reliability of comparative genomic hybridization to detect chromosome abnormalities in first polar bodies and metaphase II oocytes. | Q50672829 | ||
| Multicolour FISH detects frequent chromosomal mosaicism and chaotic division in normal preimplantation embryos from fertile patients. | Q50951072 | ||
| Diagnostic efficiency, embryonic development and clinical outcome after the biopsy of one or two blastomeres for preimplantation genetic diagnosis. | Q51968796 | ||
| Cleavage anomalies in early human embryos and survival after prolonged culture in-vitro. | Q52144237 | ||
| Paternal age and maternal age are risk factors for miscarriage; results of a multicentre European study. | Q52940098 | ||
| Maternal age, morphology, development and chromosome abnormalities in over 6000 cleavage-stage embryos. | Q53552393 | ||
| Embryo morphology and development are dependent on the chromosomal complement. | Q53586766 | ||
| Guidelines for good practice in PGD: programme requirements and laboratory quality assurance. | Q54714247 | ||
| The combination of polar body and embryo biopsy does not affect embryo viability | Q57001976 | ||
| Double locus analysis of chromosome 21 for preimplantation genetic diagnosis of aneuploidy | Q57006868 | ||
| Increased efficiency of preimplantation genetic diagnosis for infertility using “no result rescue” | Q57779224 | ||
| Removal of 2 cells from cleavage stage embryos is likely to reduce the efficacy of chromosomal tests that are used to enhance implantation rates | Q57779232 | ||
| Substandard application of preimplantation genetic screening may interfere with its clinical success | Q57779238 | ||
| Preimplantation genetic diagnosis for translocations | Q57779244 | ||
| Preimplantation genetic diagnosis significantly reduces pregnancy loss in infertile couples: a multicenter study | Q57779247 | ||
| PGD analysis for aneuploidy in a patient heterozygous for a polymorphism of chromosome 16(16qh−) | Q57779301 | ||
| Preimplantation genetic diagnosis as both a therapeutic and diagnostic tool in assisted reproductive technology | Q57779321 | ||
| Scoring criteria for preimplantation genetic diagnosis of numerical abnormalities for chromosomes X, Y, 13, 16, 18 and 21 | Q57779450 | ||
| Treatment-related chromosome abnormalities in human embryos | Q57779469 | ||
| Comparative genomic hybridization for molecular cytogenetic analysis of solid tumors | Q29618818 | ||
| Comparative genomic hybridization analysis of human oocytes and polar bodies | Q30815751 | ||
| Comparison of the results of human embryo biopsy and outcome of PGD after zona drilling using acid Tyrode medium or a laser | Q30976958 | ||
| Comparison of effects of zona drilling by non-contact infrared laser or acid Tyrode's on the development of human biopsied embryos as revealed by blastomere viability, cytoskeletal analysis and molecular cytogenetics | Q33231802 | ||
| Recent advances and future developments in PGD. | Q33830561 | ||
| Positive outcome after preimplantation diagnosis of aneuploidy in human embryos. | Q33872742 | ||
| Preimplantation diagnosis for aneuploidies in patients undergoing in vitro fertilization with a poor prognosis: identification of the categories for which it should be proposed. | Q33880192 | ||
| Outcome of preimplantation genetic diagnosis of translocations | Q33944569 | ||
| Incidence and timing of pregnancy losses: relevance to evaluating safety of early prenatal diagnosis | Q34203045 | ||
| The use of first polar bodies for preimplantation diagnosis of aneuploidy | Q34303308 | ||
| Comparison of blastocyst transfer with or without preimplantation genetic diagnosis for aneuploidy screening in couples with advanced maternal age: a prospective randomized controlled trial. | Q34357019 | ||
| Preimplantation genetic diagnosis reduces pregnancy loss in women aged 35 years and older with a history of recurrent miscarriages. | Q34440975 | ||
| Fluorescence in situ hybridization reanalysis of day-6 human blastocysts diagnosed with aneuploidy on day 3. | Q34465927 | ||
| Developmental ability of chromosomally abnormal human embryos to develop to the blastocyst stage | Q34517295 | ||
| Recurrent miscarriage: a defect in nature's quality control? | Q34768976 | ||
| Influence of past reproductive performance on risk of spontaneous abortion | Q35715568 | ||
| FISH preimplantation diagnosis of chromosome aneuploidy in recurrent pregnancy wastage | Q36267639 | ||
| Discordance among blastomeres renders preimplantation genetic diagnosis for aneuploidy ineffective | Q36268960 | ||
| Chromosome abnormalities and their relationship to morphology and development of human embryos | Q36396448 | ||
| Preimplantation genetic testing: a Practice Committee opinion | Q36975085 | ||
| Increased susceptibility to maternal aneuploidy demonstrated by comparative genomic hybridization analysis of human MII oocytes and first polar bodies | Q40276706 | ||
| A longitudinal study of pregnancy outcome following idiopathic recurrent miscarriage | Q40791097 | ||
| Survival rate of human oocytes and pregnancy outcome after vitrification using slush nitrogen in assisted reproductive technologies | Q41612743 | ||
| Poor oocyte quality rather than implantation failure as a cause of age-related decline in female fertility | Q42614542 | ||
| Nuclear transfer for full karyotyping and preimplantation diagnosis for translocations | Q44241542 | ||
| Blastomere fixation techniques and risk of misdiagnosis for preimplantation genetic diagnosis of aneuploidy | Q44412800 | ||
| Towards a full karyotype screening of interphase cells: 'FISH and chip' technology | Q46087360 | ||
| Increased Maternal Age and the Risk of Fetal Death | Q46361888 | ||
| Cytoplasmic fragmentation in activated eggs occurs in the cytokinetic phase of the cell cycle, in lieu of normal cytokinesis, and in response to cytoskeletal disorder | Q46465708 | ||
| Aneuploidy in the miscarriages of infertile women and the potential benefit of preimplanation genetic diagnosis | Q46616152 | ||
| Differences in chromosome susceptibility to aneuploidy and survival to first trimester | Q47226926 | ||
| Aneuploidy study of human oocytes first polar body comparative genomic hybridization and metaphase II fluorescence in situ hybridization analysis. | Q48808126 | ||
| High frequency of chromosomal abnormalities in embryos obtained from oocyte donation cycles | Q48822070 | ||
| Chromosome abnormalities in 1255 cleavage-stage human embryos | Q48827038 | ||
| Day 3 and day 5 morphological predictors of embryo viability | Q48829283 | ||
| Chromosome mosaicism in cleavage-stage human embryos: evidence of a maternal age effect | Q48829983 | ||
| First clinical application of comparative genomic hybridization and polar body testing for preimplantation genetic diagnosis of aneuploidy | Q48852165 | ||
| Chromosomal abnormalities in the first and second polar body. | Q48877812 | ||
| P433 | issue | 5 | |
| P921 | main subject | pregnancy outcome | Q66057507 |
| P304 | page(s) | 635-646 | |
| P577 | publication date | 2008-09-01 | |
| P1433 | published in | Expert Review of Obstetrics and Gynecology | Q15751854 |
| P1476 | title | Improving pregnancy outcome for IVF patients with preimplantation genetic screening | |
| P478 | volume | 3 |
Search more.