8 results on '"Patassini, C"'
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2. P–530 The use of wide thresholds for detecting intermediate chromosomal CNV up to 80% doesn’t improve PGT-A ability to discriminate true mosaic from uniformly aneuploid embryos
3. P–536 Validation of a Next Generation Sequencing (NGS) workflow integrating simultaneous analysis of ploidy, microdeletions and de novo monogenic diseases for expanded preimplantation genetic testing (PGT)
4. P-536 Pre-selected for an award: Validation of a Next Generation Sequencing (NGS) workflow integrating simultaneous analysis of ploidy, microdeletions and de novo monogenic diseases for expanded preimplantation genetic testing (PGT)
5. Clinical validity and utility of preconception expanded carrier screening for the management of reproductive genetic risk in IVF and general population
6. O-266 Molecular karyotyping of human single sperm by array- comparative genomic hybridization
7. Session 68: The impact of genetics in andrology
8. Seminal and molecular evidence that sauna exposure affects human spermatogenesis
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