| 13:30-13:55 | 专题报告 |
神经系统变性病的遗传机制 |
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| 13:55-14:20 | 专题报告 |
Genetic basis of pregnancy-associated decreased platelet counts and gestational thrombocytopenia |
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| 14:20-14:30 | 论文发言 |
PAX1基因新发杂合变异拓展耳-面-颈综合征2型基因型与临床表型谱 |
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| 14:30-14:40 | 论文发言 |
中国南方211例儿童Prader-Willi综合征遗传学研究 |
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| 14:40-14:50 | 论文发言 |
两种分子遗传技术联合应用快速分析流产组织染色体异常 |
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| 14:50-15:00 | 论文发言 |
Clinical Application of Preconception Expanded Carrier Screening in Populations Requiring Assisted Reproductive Technology |
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| 15:00-15:10 | 论文发言 |
Clinical outcomes of preimplantation genetic testing for structural rearrangements in couples with chromosomal inversions: a retrospective analysis |
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| 15:10-15:20 | 论文发言 |
Recurrent Paroxysmal Neurological Deficits in a 12-Year-Old Girl: A Case Report of Primary Central Nervous System Vasculitis Overlapping with MOG Antibody-Associated Disease |
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| 15:20-15:30 | 论文发言 |
Clinical Utility of Copy Number Variant Analysis Using Whole-Exome Sequencing Data: A Retrospective Study |
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