| P2093 | author name string | Richard T Scott | |
| | Nathan R Treff | |
| | Xin Tao | |
| | Yiping Zhan | |
| | Agnieszka Lonczak | |
| | David Goodrich | |
| | Jessica Landis | |
| | Rebekah Zimmerman | |
| | Tongji Xing | |
| P2860 | cites work | Development and validation of an accurate quantitative real-time polymerase chain reaction-based assay for human blastocyst comprehensive chromosomal aneuploidy screening | Q39395214 |
| | Comprehensive chromosome screening alters traditional morphology-based embryo selection: a prospective study of 100 consecutive cycles of planned fresh euploid blastocyst transfer | Q39409658 |
| | Distribution patterns of segmental aneuploidies in human blastocysts identified by next-generation sequencing. | Q46127549 |
| | Comprehensive chromosome screening is highly predictive of the reproductive potential of human embryos: a prospective, blinded, nonselection study | Q46879263 |
| | Blastocyst biopsy with comprehensive chromosome screening and fresh embryo transfer significantly increases in vitro fertilization implantation and delivery rates: a randomized controlled trial | Q48623792 |
| | The challenge of embryonic mosaicism in preimplantation genetic screening. | Q53184585 |
| | Validation of copy number variation sequencing for detecting chromosome imbalances in human preimplantation embryos. | Q54200763 |
| | Use of single nucleotide polymorphism microarrays to distinguish between balanced and normal chromosomes in embryos from a translocation carrier. | Q54372768 |
| | Validation of a semiconductor next-generation sequencing-based protocol for preimplantation genetic diagnosis of reciprocal translocations | Q85729102 |
| | The origin, mechanisms, incidence and clinical consequences of chromosomal mosaicism in humans | Q34411991 |
| | Accurate single cell 24 chromosome aneuploidy screening using whole genome amplification and single nucleotide polymorphism microarrays | Q34617227 |
| | Single embryo transfer with comprehensive chromosome screening results in improved ongoing pregnancy rates and decreased miscarriage rates | Q35829512 |
| | Human embryos commonly form abnormal nuclei during development: a mechanism of DNA damage, embryonic aneuploidy, and developmental arrest | Q35856560 |
| | Using SNP array to identify aneuploidy and segmental imbalance in translocation carriers | Q35951201 |
| | Selection of single blastocysts for fresh transfer via standard morphology assessment alone and with array CGH for good prognosis IVF patients: results from a randomized pilot study | Q36112761 |
| | Identification of small segmental translocations in patients with repeated implantation failure and recurrent miscarriage using next generation sequencing after in vitro fertilization/intracytoplasmic sperm injection | Q36416984 |
| | Chromosomal microarray versus karyotyping for prenatal diagnosis | Q36546668 |
| | Clinical application of next-generation sequencing in preimplantation genetic diagnosis cycles for Robertsonian and reciprocal translocations | Q37059987 |
| | A randomized and blinded comparison of qPCR and NGS-based detection of aneuploidy in a cell line mixture model of blastocyst biopsy mosaicism | Q37444800 |
| | The nature of aneuploidy with increasing age of the female partner: a review of 15,169 consecutive trophectoderm biopsies evaluated with comprehensive chromosomal screening | Q38172667 |
| | SNP array-based analyses of unbalanced embryos as a reference to distinguish between balanced translocation carrier and normal blastocysts. | Q38860681 |
| P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
| P6216 | copyright status | copyrighted | Q50423863 |
| P433 | issue | 8 | |
| P304 | page(s) | 975-981 | |
| P577 | publication date | 2017-06-02 | |
| P1433 | published in | Journal of Assisted Reproduction and Genetics | Q15755113 |
| P1476 | title | Evaluation of comprehensive chromosome screening platforms for the detection of mosaic segmental aneuploidy | |
| P478 | volume | 34 | |