Venue
NSGC 2019
Topic |
Session |
Date / Time / Location |
|
| 1 | Customer Experience: Online Ordering and Financial Assistance Policy | Nov. 6 12:00pm – 12:15pm Exhibit Hall, Booth #201 |
|
| 2 | Product Updates: GeneAware, Hereditary Cancer | Nov. 6 12:30pm – 12:45pm Exhibit Hall, Booth #201 |
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| 3 | Customer Experience: Online Ordering and Financial Assistance Policy | Nov. 6 6:00pm – 6:15pm Exhibit Hall, Booth #201 |
|
| 4 | Product Updates: GeneAware, Hereditary Cancer | Nov. 6 6:30pm – 6:45pm Exhibit Hall, Booth #201 |
|
| 5 | Customer Experience: Online Ordering and Financial Assistance Policy | Nov. 7 11:45am – 12:00pm Exhibit Hall, Booth #201 |
|
| 6 | Product Updates: GeneAware, Hereditary Cancer | Nov. 7 12:15pm – 12:30pm Exhibit Hall, Booth #201 |
|
| 7 | Customer Experience: Online Ordering and Financial Assistance Policy | Nov. 7 1:00pm – 1:15pm Exhibit Hall, Booth #201 |
|
| 8 | Product Updates: GeneAware, Hereditary Cancer | Nov. 7 1:30pm – 1:45pm Exhibit Hall, Booth #201 |
Title |
Author |
Type / Poster # |
Date / Time / Location |
|
| 1 | Clinical Utility of a 12-gene Noonan Spectrum Disorders Panel in Prenatal and Postnatal Cohorts | Zhao Chen, Ph.D. | POSTER // #543 Prenatal, Perinatal, Reproductive, and Developmental Genetics |
Oct. 16 2:00 pm – 3:00 pm Exhibit Hall |
| 2 | Phenotypic Expansion of TAF1-related Syndrome: TAF1 Variants and Clinical Phenotypes | Hanyin Cheng, Fellow | POSTER // #597 Prenatal, Perinatal, Reproductive, and Developmental Genetics |
Oct. 16 2:00 pm – 3:00 pm Exhibit Hall |
| 3 | Haploinsufficiency of PRR12 Causes a Congenital Multiple-malformation Neurodevelopmental Syndrome with a Wide Phenotypic Spectrum | Weimin Bi, Ph.D. | POSTER // #2553 Molecular and Cytogenetic Diagnostics |
Oct. 16 2:00 pm – 3:00 pm Exhibit Hall |
| 4 | New Cases with “CNV-mutator” Phenotype Characterized by Concurrent de Novo NAHR-mediated Deletion Events | Bo Yuan, Ph.D. | POSTER // #3102 Molecular Effects of Genetic Variation |
Oct. 16 3:00 pm – 4:00 pm Exhibit Hall |
| 5 | Clinical Validation and Implementation of Whole Genome Sequencing in Molecular Diagnostics of Mendelian Disorders | Yue Wang, Ph.D. | POSTER // #545 Prenatal, Perinatal, Reproductive, and Developmental Genetics |
Oct. 17 3:00 pm – 4:00 pm Exhibit Hall |
| 6 | Game of Exomes: Comparing Sequencing of Commercial Laboratories in the Undiagnosed Disease Network | Hongzheng Dai, Ph.D | POSTER // #2608 Molecular and Cytogenetic Diagnostics |
Oct. 17 3:00 pm – 4:00 pm Exhibit Hall |
| 7 | Haploinsufficiency of PRR12 Causes a Congenital Multiple-malformation Neurodevelopmental Syndrome with a Wide Phenotypic Spectrum | Weimin Bi, Ph.D. | POSTER // #545 Prenatal, Perinatal, Reproductive, and Developmental Genetics |
Oct. 18 1:00 pm – 2:00 pm Exhibit Hall |
| 8 | A Novel Next-Generation Sequencing Platform for Hereditary Cancer Risk Evaluation | Jun Yang, Ph.D. | POSTER // #977 Cancer Genetics |
Oct. 18 1:00 pm – 2:00 pm Exhibit Hall |
| 9 | Identification of an Insertional Duplication of the AMT Gene in a Patient with Glycine Encephalopathy | Lei Wang, Ph.D. | POSTER // #2507 Molecular and Cytogenetic Diagnostics |
Oct. 18 1:00 pm – 2:00 pm Exhibit Hall |
| 10 | Development of a Clinical Summary Tool that Reduces Clinical Note Review Time and Standardizes Phenotype Terminology | Jason Salvo, Ph.D. | POSTER // #1706 Bioinformatics and Computational Approaches |
Oct. 18 2:00 pm – 3:00 pm Exhibit Hall |