...
机译:使用记录链接和手动随访评估维多利亚氏母体唐氏综合症,18三体性和神经管缺陷的血清筛查四联检查
Alice M Jaques, Research Officer, Public Health Genetics, MurdochChildrens Research Institute, Royal Children’s Hospital;
Department ofPaediatrics, The University of Melbourne, Australia.Veronica R Collins, Epidemiologist, Public Health Genetics, MurdochChildrens Research Institute, Royal Children’s Hospital, Australia.Kerry Haynes, Research Assistant, Public Health Genetics, MurdochChildrens Research Institute, Royal Children’s Hospital, Australia.Leslie J Sheffield, Senior Clinical Geneticist, Department of Paediatrics,The University of Melbourne, Melbourne, Australia;
GeneticHealth Services Victoria, Royal Children’s Hospital, Australia;
MurdochChildrens Research Institute, Royal Children’s Hospital, Australia.Ivan Francis, Senior Medical Scientist, Genetic Health ServicesVictoria, Royal Children’s Hospital, Australia.Robin Forbes, Clinical Services Manager, Genetic Health ServicesVictoria, Royal Children’s Hospital, Australia.Jane L Halliday, Head, Public Health Genetics, Murdoch ChildrensResearch Institute, Royal Children’s Hospital;
Department of Paediatrics,The University of Melbourne, Melbourne, Australia;
Birth DefectsRegister, Department of Human Services, Melbourne, Victoria, Australia.;
机译:使用记录链接和手动随访评估维多利亚氏母体血清筛查四联试验对唐氏综合症,18三体性和神经管缺陷
机译:孕妇血清筛查唐氏综合症,开放性神经管缺损和三体性18。
机译:孕妇前期孕妇的三术21,18和开放神经管缺陷(ONTD)的新截止值
机译:在先前怀孕的筛查阳性结果后参与唐氏综合症神经管畸形和18三体性的孕妇血清筛查
机译:在先前怀孕的筛查阳性结果后,参与唐氏综合症,神经管畸形和18三体性的孕妇血清筛查