安心交易
不成功退款，无后顾之忧，风险服务升级。
The aim of the journal is to communicate the results of original research in a variety of clinical and scientific specialities concerned with in utero diagnosis of fetal abnormality in man (and animal models) resulting from genetic and environmental factors. This is considered to encompass: genetic and other forms of screening aimed at identifying pregnancies at risk of fetal abnormality the epidemiology and pathology of fetal abnormality (including fetal infection) fetal and maternal factors relating to intrauterine development antenatal care in relation to the prevention of fetal abnormality genetic counselling and selective termination of pregnancy psychosocial aspects of prenatal diagnosis the development and evaluation of services for prenatal diagnosis developments in the field of obstetric ultrasound amniocentesis chorion villus sampling fetoscopy and fetal blood and tissue sampling medical and surgical treatment of fetal disorders developments in genetic linkage and DNA analysis for the diagnosis of gene mutations diagnosis of metabolic defects from chorion villus samples and amniotic fluid advances in amniotic cell culture and cytogenetic techniques pre-implantation diagnosis first trimester maternal serum screening and early amniocentesis multicolour fluorescence in situ analysis for aneuploidy detection in interphase isolation and analysis of fetal cells from the maternal circulation Editorial Policy The overriding criteria for publication are originality a high scientific quality and interest to a wide audience of those concerned with all aspects of prenatal diagnosis research. The journal provides a multidisciplinary forum for the exchange of information by which it is hoped to increase knowledge about the aetiology and pathogenesis of fetal abnormality and to promote further opportunities for its treatment and prevention. Papers not sufficiently substantiated by experimental detail will not be accepted and although technical queries will be referred back to the author the Editor reserves the right to make alterations in the text without altering the technical content.
本杂志的目的是将原始研究的结果传达给各种临床和科学专业，这些专业涉及由遗传和环境因素引起的人类（和动物模型）胎儿异常的宫内诊断。这被认为包括：基因和其他形式的筛查，目的是鉴别有胎儿异常风险的妊娠胎儿异常的流行病学和病理学胎儿异常（包括胎儿感染）的流行病学和病理学胎儿和母亲与宫内发育有关的因素产前护理与预防胎儿异常有关的遗传妊娠咨询和选择性终止产前诊断的心理社会方面产科超声羊膜穿刺术、绒毛取样、胎儿镜和胎儿血液组织取样、医学和外科治疗胎儿疾病的发展和产前诊断服务的发展和评价绒毛膜绒毛和羊水代谢缺陷的基因连锁分析和DNA分析诊断羊水细胞培养和细胞遗传学技术在植入前诊断、孕早期母体血清筛查和早期羊膜穿刺多色荧光原位肛门中的进展从《母体循环》社论政策中分离和分析胎儿细胞的间期非整倍体检测，出版的首要标准是独创性、高科学性和广泛关注产前诊断研究各个方面的人群的兴趣。该杂志提供了一个多学科的信息交流论坛，希望借此增进对胎儿畸形病因和发病机制的了解，并促进进一步的治疗和预防机会。未经实验细节充分证实的论文将不被接受，尽管技术问题将反馈给作者，但编辑保留在不改变技术内容的情况下修改文本的权利。
安心交易
不成功退款，无后顾之忧，风险服务升级。
合规备案认证机构
资质许可齐全，合规经营，用户权益有保障。
正刊保障
刊物在国家新闻出版署网可查，抵制假刊、增刊。
对公账户资金监管
交易均通过对公账户，资金安全有保障。01 选择服务并上传稿件 我们的学术顾问将根据您的需求推荐适合的服务
02 分配资深编辑和同行专家 根据您的服务方案和研究方向，为您分配资深编辑和同行专家
03 交付及反馈 每个环节的服务会在您审阅和确认后进行下一步，根据您的反馈和建议做调整
04 提升稿件质量 我们将基于您的反馈并平衡期刊的投稿要求，为您进一步优化稿件
05 提交投稿 出版专家将在您确认定稿后，为您整理并检查所有必须文件，协助您完成期刊投稿。
06 投稿跟进 及时查询稿件状态，协助您与期刊编辑沟通，根据审稿意见协助修正文章
07 拒稿支持 若期刊拒稿，您可通过拒稿咨询服务发掘稿件的改进方案，并获取365天无限次向同期刊或其他期刊的重投服务
