Keywords: تشخیص پیش از تولد; chromosome; deletion; prenatal diagnosis; ultrasound
مقالات ISI تشخیص پیش از تولد (ترجمه نشده)
مقالات زیر هنوز به فارسی ترجمه نشده اند.
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در صورتی که به ترجمه آماده هر یک از مقالات زیر نیاز داشته باشید، می توانید سفارش دهید تا مترجمان با تجربه این مجموعه در اسرع وقت آن را برای شما ترجمه نمایند.
Keywords: تشخیص پیش از تولد; Multicystic dysplastic kidney; Contralateral anomalies; Nephrectomy; Child; Prenatal diagnosis
Keywords: تشخیص پیش از تولد; Omphalocele; Perinatal outcome; Prenatal diagnosis; Counseling; Abdominal wall defect;
Keywords: تشخیص پیش از تولد; Congenital diaphragmatic hernia; CDH study group; Registry; Prenatal diagnosis; Diaphragmatic defect; Extracorporeal membrane oxygenation; Outcomes
Keywords: تشخیص پیش از تولد; Congenital malformations; Prenatal diagnosis; Ultrasound diagnosis; Epidemiology of birth defects; Congenital heart defects;
Keywords: تشخیص پیش از تولد; placenta accreta; prenatal diagnosis; sensitivity and specificity; ultrasound;
Keywords: تشخیص پیش از تولد; complete hydatidiform mole; dizygotic twin; intrauterine insemination; microsatellite genotyping; prenatal diagnosis
Keywords: تشخیص پیش از تولد; Fetal surgery; Hindbrain herniation; Hydrocephalus; Myelomeningocele; Prenatal diagnosis; Spina bifida
Keywords: تشخیص پیش از تولد; first-trimester screen; noninvasive prenatal testing; prenatal diagnosis; prenatal screening;
Keywords: تشخیص پیش از تولد; MRI; safety; prenatal diagnosis; indication;
Keywords: تشخیص پیش از تولد; Amniocentesis; Aneuploidías; Pruebas genéticas; Diagnóstico prenatal; Guía prácticaAmniocentesis; Aneuploidies; Genetic testing; Prenatal diagnosis; Practice guideline
Keywords: تشخیص پیش از تولد; Prenatal diagnosis; Constitutional bone diseases; 2D ultrasound; CT
Keywords: تشخیص پیش از تولد; Clinical management; Congenital diaphragmatic hernia; Prenatal diagnosis; Pulmonary hypertension; Ventilation
Keywords: تشخیص پیش از تولد; Prenatal diagnosis; Abortion; Amniocentesis; Chromosomes; Ultrasound; Down syndrome;
Keywords: تشخیص پیش از تولد; Human karyotype; Amniocentesis; Prenatal diagnosis; Down's syndrome cytogenetics; History of medical genetics; Madrid (Spain);
Keywords: تشخیص پیش از تولد; Non-invasive prenatal testing; cell free fetal DNA; ethics; policy; prenatal diagnosis; prenatal screening;
Keywords: تشخیص پیش از تولد; prenatal diagnosis; renal tract anomalies; ultrasound
Keywords: تشخیص پیش از تولد; twin pregnancy; ultrasound; prenatal diagnosis
Keywords: تشخیص پیش از تولد; Urethral obstruction; Prenatal diagnosis; Prune-belly syndrome; Prenatal ultrasonography; Posterior urethral valves; Fetal intervention;
Keywords: تشخیص پیش از تولد; Carrier testing; Homozygous deletions; Prenatal diagnosis; spinal muscular atrophy; SMN1;
Keywords: تشخیص پیش از تولد; Pregnancy; Conjoined twins; Ultrasonography; Fetal echocardiography; Prenatal diagnosis; STIC; Spatiotemporal image correlation;
Keywords: تشخیص پیش از تولد; clinical variables; congenital anomaly; disclosure; gender differences; parental emotional reactions; prenatal diagnosis; postnatal diagnosis;
Keywords: تشخیص پیش از تولد; Prenatal diagnosis; Congenital abnormalities; CT scan; Doppler ultrasoundDiagnóstico pré-natal; Anormalidades congênitas; Tomografia computadorizada; Ultrassonografia Doppler
Keywords: تشخیص پیش از تولد; ROS; Antioxidants; Autophagy; Cancer; Cleft lip/palate; Prenatal diagnosis
Keywords: تشخیص پیش از تولد; 22q11.2 deletion; prenatal diagnosis; right aortic arch
Keywords: تشخیص پیش از تولد; Quantitative fluorescent polymerase chain reaction (QF-PCR); Chromosomal microarray (CMA); Genomic imbalance; Nuchal translucency; Prenatal diagnosis
Keywords: تشخیص پیش از تولد; Congenital diaphragmatic hernia; Quantitative lung index; Neonatal mortality; Prenatal diagnosis; Fetal surgery; Lung hypoplasia
Keywords: تشخیص پیش از تولد; Nager syndrome; Acrofacial dysostosis; Chromosomal microarray; Prenatal diagnosis; SF3B4
Keywords: تشخیص پیش از تولد; Prenatal diagnosis; Mitochondrial trifunctional protein (TFP); Acylcarnitine analysis; Fatty acid oxidation; HADHA geneHADHA OMIM: 600890, GDB: 434026, GenBank: NM_000182; HADHB OMIM: 143450, GDB: 344953, GenBank: NM_000183
Keywords: تشخیص پیش از تولد; aCGH; chromosome 8p inverted duplication deletion syndrome; inv dup del(8p); prenatal diagnosis; ultrasound
Keywords: تشخیص پیش از تولد; cystic hygroma; 5p deletion; 7p duplication; prenatal diagnosis; ventriculomegaly
Keywords: تشخیص پیش از تولد; Cleft lip; Cleft palate; Incidence; Prenatal diagnosis
Keywords: تشخیص پیش از تولد; 9p deletion syndrome; 14q duplication syndrome; partial monosomy 9p; partial trisomy 14q; prenatal diagnosis
Keywords: تشخیص پیش از تولد; Gastroschisis; Prenatal diagnosis; Abdominal wall defects; Congenital malformations; Fetal ultrasound
Prenatal diagnosis of fetal glutaric aciduria type 1 with rare compound heterozygous mutations in GCDH gene
Keywords: تشخیص پیش از تولد; Glutaric aciduria type 1; GCDH gene mutation; Prenatal diagnosis; Compound heterozygous gene mutation;
Clinical and submicroscopic findings of two prenatal cases with inv dup del(8p) syndrome
Keywords: تشخیص پیش از تولد; ARHGEF10; Rho guanine nucleotide exchange factor 10; Array CGH; Array comparative genomic hybridization; ASD; Atrial septal defect; CCA; Corpus callosum abnormality; CVA; Cerebellar vermis agenesis; dic(8); Dicentric chromosome 8; FISH; Fluorescence in si
Prenatal diagnosis of hydrancephaly and enlarged cerebellum and cisterna magna in a fetus with thanatophoric dysplasia type II and a review of prenatal diagnosis of brain anomalies associated with thanatophoric dysplasia
Keywords: تشخیص پیش از تولد; Brain anomalies; Hydrancephaly; Prenatal diagnosis; Thanatophoric dysplasia type II;
Desirable quality-control materials for the establishment of qualified external quality assessment on prenatal diagnosis of chromosomal aneuploidies
Keywords: تشخیص پیش از تولد; Fluorescence in situ hybridization; External quality assessment; Prenatal diagnosis; Chromosomal aneuploidies; Quality control materials;
Prenatal diagnosis of a 0.7-Mb 17p13.3 microdeletion encompassing YWHAE and CRK but not PAFAH1B1 in a fetus without ultrasound abnormalities
Keywords: تشخیص پیش از تولد; 17p13.3 microdeletion; CRK; PAFAH1B1; Prenatal diagnosis; YWHAE;
Quels sont l'objectif réel et la portée du dépistage des aneuploïdies ?
Keywords: تشخیص پیش از تولد; Dépistage prénatal non invasif; Dépistage par marqueurs multiples; Dépistage de l'ADN libre circulant; Dépistage des aneuploïdie; Diagnostic prénatal; Non-invasive prenatal screening; Multiple marker screening; Cell-free DNA screening; Aneuploidy
Adverse Perinatal Conditions Associated With Prenatally Detected Fetal Echogenic Bowel in Nova Scotia
Keywords: تشخیص پیش از تولد; Echogenic bowel; adverse perinatal outcomes; prenatal diagnosis; CF; cystic fibrosis; CMV; cytomegalovirus; FATC; Fetal Assessment and Treatment Centre; IUGR; intrauterine growth restriction;
Anomalie de rotation rénale entraînant une hydronéphrose géante prénatale
Keywords: تشخیص پیش از تولد; Renal malrotation; Hydronephrosis; Prenatal diagnosis;
First prenatal case of proximal 19p13.12 microdeletion syndrome: New insights and new delineation of the syndrome
Keywords: تشخیص پیش از تولد; Proximal 19p13.12 microdeletion; Prenatal diagnosis; Novel critical interval; Branchial arch defects; Contiguous gene deletion syndrome;
Whole exome sequencing identifies a pathogenic mutation in WFS1 in two large Chinese families with autosomal dominant all-frequency hearing loss and prenatal counseling
Keywords: تشخیص پیش از تولد; WFS1; All-frequency sensorineural hearing loss; Prenatal diagnosis; Autosomal dominant; WES;
Human embryonic curvature studied with 3D ultrasound in ongoing pregnancies and miscarriages
Keywords: تشخیص پیش از تولد; 3D ultrasound; Early pregnancy; Embryonic curvature; Prenatal diagnosis;
Beckwith Wiedemann syndrome: A population-based study on prevalence, prenatal diagnosis, associated anomalies and survival in Europe
Keywords: تشخیص پیش از تولد; Beckwith Wiedemann syndrome; Congenital anomalies; Prenatal diagnosis; Epidemiology; Europe;
Prenatal therapy with pyrimethamine + sulfadiazine vs spiramycin to reduce placental transmission of toxoplasmosis: a multicenter, randomized trial
Keywords: تشخیص پیش از تولد; pregnancy; prenatal diagnosis; pyrimethamine-sulfadiazine; spiramycin; tolerance; toxoplasmosis;
Dilemmas in genetic counseling for low-penetrance neuro-susceptibility loci detected on prenatal chromosomal microarray analysis
Keywords: تشخیص پیش از تولد; chromosomal microarray analysis; copy number variant; genetic counseling; prenatal diagnosis; variant of uncertain significance; low-penetrance neuro-susceptibility loci;
Cell-Free DNA
Keywords: تشخیص پیش از تولد; Prenatal diagnosis; cfDNA; Noninvasive prenatal testing; Single-gene disorders; Prenatal screening; Rhesus D genotype;
Placenta accreta spectrum: pathophysiology and evidence-based anatomy for prenatal ultrasound imaging
Keywords: تشخیص پیش از تولد; cesarean delivery; increta; percreta; placenta accrete; prenatal diagnosis; ultrasound imaging;