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机译:父母外壳测序诊断致死或产前发作常染色体隐性障碍
Molecular Genetics DepartmentRoyal Devon and Exeter NHS Foundation TrustExeter UK;
Institute of Biomedical and Clinical ScienceUniversity of Exeter Medical SchoolExeter UK;
Molecular Genetics DepartmentRoyal Devon and Exeter NHS Foundation TrustExeter UK;
Institute of Biomedical and Clinical ScienceUniversity of Exeter Medical SchoolExeter UK;
Molecular Genetics DepartmentRoyal Devon and Exeter NHS Foundation TrustExeter UK;
Clinical Genetics DepartmentRoyal Devon and Exeter NHS Foundation TrustExeter UK;
Molecular Genetics DepartmentRoyal Devon and Exeter NHS Foundation TrustExeter UK;
Molecular Genetics DepartmentRoyal Devon and Exeter NHS Foundation TrustExeter UK;
Molecular Genetics DepartmentRoyal Devon and Exeter NHS Foundation TrustExeter UK;
Institute of Biomedical and Clinical ScienceUniversity of Exeter Medical SchoolExeter UK;
Department of Clinical GeneticsOur Lady's Children's HospitalDublin Ireland;
North West Thames Regional Genetics ServiceLondon North West Healthcare NHS TrustHarrow UK;
Guy's Regional Genetics ServiceGuy's and St Thomas' NHS Foundation TrustLondon UK;
Oxford Regional Clinical Genetics ServiceNorthampton General HospitalNorthampton UK;
Clinical Genetics DepartmentRoyal Devon and Exeter NHS Foundation TrustExeter UK;
Oxford Centre for Genomic MedicineOxford University Hospitals NHS Foundation TrustOxford UK;
West Midlands Medical Genetics DepartmentBirmingham Women's HospitalBirmingham UK;
Guy's Regional Genetics ServiceGuy's and St Thomas' NHS Foundation TrustLondon UK;
Department of Clinical Genetics City CampusNottingham University Hospitals NHS TrustNottingham UK;
Department of Clinical Genetics City CampusNottingham University Hospitals NHS TrustNottingham UK;
South West Thames Regional Genetics ServiceSt George's University Hospitals NHS Foundation;
Institute of Medical GeneticsUniversity Hospital of WalesCardiff UK;
Department of Clinical GeneticsLiverpool Women's NHS Foundation TrustLiverpool UK;
Guy's Regional Genetics ServiceGuy's and St Thomas' NHS Foundation TrustLondon UK;
South West Thames Regional Genetics ServiceSt George's University Hospitals NHS Foundation;
Clinical Genetics DepartmentRoyal Devon and Exeter NHS Foundation TrustExeter UK;
Department of Clinical GeneticsLiverpool Women's NHS Foundation TrustLiverpool UK;
Department of Clinical GeneticsUniversity Hospital BristolBristol UK;
Sheffield Clinical Genetics ServiceSheffield Children's HospitalSheffield UK;
Victorian Clinical Genetics ServicesMurdoch Children's Research InstituteMelbourne Vic Australia;
Department of Clinical Genetics City CampusNottingham University Hospitals NHS TrustNottingham UK;
Department of Clinical Genetics City CampusNottingham University Hospitals NHS TrustNottingham UK;
Oxford Centre for Genomic MedicineOxford University Hospitals NHS Foundation TrustOxford UK;
Department of Clinical GeneticsUniversity Hospital BristolBristol UK;
Guy's Regional Genetics ServiceGuy's and St Thomas' NHS Foundation TrustLondon UK;
Clinical Genetics DepartmentRoyal Devon and Exeter NHS Foundation TrustExeter UK;
Institute of Medical GeneticsUniversity Hospital of WalesCardiff UK;
Leicester Clinical Genetics Women's and Children's ServicesLeicester Royal InfirmaryLeicester UK;
Guy's Regional Genetics ServiceGuy's and St Thomas' NHS Foundation TrustLondon UK;
Institute of Biomedical and Clinical ScienceUniversity of Exeter Medical SchoolExeter UK;
Molecular Genetics DepartmentRoyal Devon and Exeter NHS Foundation TrustExeter UK;
机译:父母外壳测序诊断致死或产前发作常染色体隐性障碍
机译:一个家庭中两种常染色体隐性遗传疾病的全外显子测序诊断
机译:外显子组测序确定KIF14中的突变是常染色体隐性致死性胎儿纤毛病表型的新原因
机译:诊断产前疾病 - 使用稳健的分析方法对母体人类等离子体的搜索生物标志物
机译:智能疾病和自闭症谱系血型术中的常染色体隐性变体
机译:通过父母外显子组测序诊断致死性或产前发作的常染色体隐性遗传疾病
机译:通过父母外显子组测序诊断致死性或产前发作的常染色体隐性遗传疾病