Prenatal Diagnosis welcomes submissions in all aspects of prenatal diagnosis with a particular focus on areas in which molecular biology and genetics interface with prenatal care and therapy, encompassing: all aspects of fetal imaging, including sonography and magnetic resonance imaging; prenatal cytogenetics, including molecular studies and array CGH; prenatal screening studies; fetal cells and cell-free nucleic acids in maternal blood and other fluids; preimplantation genetic diagnosis (PGD); prenatal diagnosis of single gene disorders, including metabolic disorders; fetal therapy; fetal and placental development and pathology; development and evaluation of laboratory services for prenatal diagnosis; psychosocial, legal, ethical and economic aspects of prenatal diagnosis; prenatal genetic counseling
产前诊断欢迎提交产前诊断的所有方面，特别是分子生物学和遗传学与产前护理和治疗相互作用的领域，包括：胎儿成像的所有方面，包括超声检查和磁共振成像;产前细胞遗传学，包括分子研究和阵列CGH;产前筛查研究;母体血液和其它流体中的胎儿细胞和无细胞核酸;植入前遗传学诊断;单基因疾病的产前诊断，包括代谢疾病;胎儿治疗;胎儿和胎盘发育和病理学;发展和评估产前诊断实验室服务;产前诊断的社会心理、法律、伦理和经济方面;产前遗传咨询
Advanced paternal age, infertility, and reproductive risks: A review of the literature
来源期刊：Prenatal DiagnosisDOI：10.1002/pd.5402
Fetal fraction and noninvasive prenatal testing: What clinicians need to know
来源期刊：Prenatal DiagnosisDOI：10.1002/pd.5620
A system‐based approach to the genetic etiologies of non‐immune hydrops fetalis
来源期刊：Prenatal DiagnosisDOI：10.1002/pd.5479
Amniotic membrane and placental histopathological findings after open and fetoscopic prenatal neural tube defect repair
来源期刊：Prenatal DiagnosisDOI：10.1002/pd.5414
The price of abandoning diagnostic testing for cell free fetal DNA screening
来源期刊：Prenatal DiagnosisDOI：10.1002/pd.5405
Noninvasive screening by cell‐free DNA for 22q11.2 deletion: Benefits, limitations, and challenges
来源期刊：Prenatal DiagnosisDOI：10.1002/pd.5391
Evaluation of a new balloon for fetal endoscopic tracheal occlusion in the nonhuman primate model
来源期刊：Prenatal DiagnosisDOI：10.1002/pd.5445
Hypoplastic nasal bone: A potential marker for facial dysmorphism associated with pathogenic copy number variants on microarray
来源期刊：Prenatal DiagnosisDOI：10.1002/pd.5410
A sonographic approach to the prenatal diagnosis of skeletal dysplasias
来源期刊：Prenatal DiagnosisDOI：10.1002/pd.5501
Fetal myelomeningocele surgery: Only treating the tip of the iceberg
来源期刊：Prenatal DiagnosisDOI：10.1002/pd.5390
Chromosomal microarray analysis in fetuses with an isolated congenital heart defect: A retrospective, nationwide, multicenter study in France
来源期刊：Prenatal DiagnosisDOI：10.1002/pd.5449
Prenatal detection of isolated bilateral hyperechogenic kidneys: Etiologies and outcomes
来源期刊：Prenatal DiagnosisDOI：10.1002/pd.5418
Current Controversies in Prenatal Diagnosis 2: NIPT results suggesting maternal cancer should always be disclosed
来源期刊：Prenatal DiagnosisDOI：10.1002/pd.5379
The use of fetal MRI for renal and urogenital tract anomalies
来源期刊：Prenatal DiagnosisDOI：10.1002/pd.5610
Prenatal genetic considerations of congenital anomalies of the kidney and urinary tract (CAKUT)
来源期刊：Prenatal DiagnosisDOI：10.1002/pd.5536
The use of magnetic resonance imaging in the prediction of birthweight
来源期刊：Prenatal DiagnosisDOI：10.1002/pd.5530
The utilization of prenatal microarray: A survey of current genetic counseling practices and barriers
来源期刊：Prenatal DiagnosisDOI：10.1002/pd.5435
Validation of fetal DNA fraction estimation and its application in noninvasive prenatal testing for aneuploidy detection in multiple pregnancies
来源期刊：Prenatal DiagnosisDOI：10.1002/pd.5597
The MRI spectrum of congenital cytomegalovirus infection
来源期刊：Prenatal DiagnosisDOI：10.1002/pd.5591
Cranial sonographic markers of fetal open spina bifida at 11 to 13 weeks of gestation
来源期刊：Prenatal DiagnosisDOI：10.1002/pd.5614
DiGeorge syndrome chromosome region deletion and duplication: Prenatal genotype‐phenotype variability in fetal ultrasound and MRI
来源期刊：Prenatal DiagnosisDOI：10.1002/pd.5572
The use of image fusion in prenatal medicine
来源期刊：Prenatal DiagnosisDOI：10.1002/pd.5558
Impact of introduction of noninvasive prenatal testing on uptake of genetic testing in fetuses with central nervous system anomalies
来源期刊：Prenatal DiagnosisDOI：10.1002/pd.5466
Current Controversies in Prenatal Diagnosis 3: Gene editing should replace embryo selection following PGD
来源期刊：Prenatal DiagnosisDOI：10.1002/pd.5442
Fetal anogenital distance using ultrasound
来源期刊：Prenatal DiagnosisDOI：10.1002/pd.5459
Fetal and perinatal outcome associated with small cerebellar diameter based on second‐ or third‐trimester ultrasonography
来源期刊：Prenatal DiagnosisDOI：10.1002/pd.5465
Metabolic fingerprinting of chorionic villous samples in normal pregnancy and chromosomal disorders
来源期刊：Prenatal DiagnosisDOI：10.1002/pd.5461
Is it feasible to select fetuses for prenatal WES based on the prenatal phenotype?
来源期刊：Prenatal DiagnosisDOI：10.1002/pd.5522
Incidence of gastro‐intestinal anomalies and surgical outcome of fetuses diagnosed with echogenic bowel and bowel dilatation
来源期刊：Prenatal DiagnosisDOI：10.1002/pd.5552
Prenatal cerebral imaging features of a new syndromic entity related to KIAA1109 pathogenic variants mimicking tubulinopathy
来源期刊：Prenatal DiagnosisDOI：10.1002/pd.5589
Placental infection of hepatitis B virus among Thai pregnant women: Clinical risk factors and its association with fetal infection
来源期刊：Prenatal DiagnosisDOI：10.1002/pd.5628
What are women saying about noninvasive prenatal testing? An analysis of online pregnancy discussion forums
来源期刊：Prenatal DiagnosisDOI：10.1002/pd.5500
Digital vs face‐to‐face information provision in patient counselling for prenatal screening: A noninferiority randomized controlled trial
来源期刊：Prenatal DiagnosisDOI：10.1002/pd.5463
Improving fetal congenital heart disease screening using a checklist‐based approach
来源期刊：Prenatal DiagnosisDOI：10.1002/pd.5581
Fetal cardiac intervention—Perspectives from a single center
来源期刊：Prenatal DiagnosisDOI：10.1002/pd.5631
Neonatal outcome of cases with isolated prenatal ventricular disproportion with a dominant right ventricle
来源期刊：Prenatal DiagnosisDOI：10.1002/pd.5567
Prenatal diagnosis and postnatal outcome of anterior urethral anomalies
来源期刊：Prenatal DiagnosisDOI：10.1002/pd.5582
Comment on “Trisomy 21 noninvasive prenatal testing for twin pregnancies”
来源期刊：Prenatal DiagnosisDOI：10.1002/pd.5456
Issue Information
来源期刊：Prenatal DiagnosisDOI：10.1002/pd.5304
A survey of current clinical practice of chorionic villus sampling
来源期刊：Prenatal DiagnosisDOI：10.1002/pd.5425
Germline mosaicism in an α‐thalassemia family: Incidental identification by prenatal ultrasound
来源期刊：Prenatal DiagnosisDOI：10.1002/pd.5534
The utility of nuchal translucency ultrasound in identifying rare chromosomal abnormalities not detectable by cell‐free DNA screening
来源期刊：Prenatal DiagnosisDOI：10.1002/pd.5583
Prenatal enzymatic diagnosis of lysosomal storage diseases using cultured amniotic cells, uncultured chorionic villus samples, and fetal blood cells: Hacettepe experience
来源期刊：Prenatal DiagnosisDOI：10.1002/pd.5547
Corrigendum for Wald NJ, Bestwick JP, Huttly WJ, Aldis J, Borrell A, Goodburn S & Mills I (2018) https://doi.org/10.1002/pd.5381
来源期刊：Prenatal DiagnosisDOI：10.1002/pd.5468
Z scores of the fetal trachea and bronchial dimension
来源期刊：Prenatal DiagnosisDOI：10.1002/pd.5394
Issue Information
来源期刊：Prenatal DiagnosisDOI：10.1002/pd.5309
Issue Information
来源期刊：Prenatal DiagnosisDOI：10.1002/pd.5306
Prognosis of fetuses with ventriculomegaly: An observational retrospective study
来源期刊：Prenatal DiagnosisDOI：10.1002/pd.5503
Pregnant women with confirmed neoplasms should not have noninvasive prenatal testing
来源期刊：Prenatal DiagnosisDOI：10.1002/pd.5544
Issue Information
来源期刊：Prenatal DiagnosisDOI：10.1002/pd.5305
