about
Array comparative genomic hybridization and fetal congenital heart defects: a systematic review and meta-analysisGenomic microarray in fetuses with increased nuchal translucency and normal karyotype: a systematic review and meta-analysisFirst-trimester screening for trisomy 21 combining biochemistry and ultrasound at individually optimal gestational ages. An interventional studyPrenatal Detection of Down Syndrome using Massively Parallel Sequencing (MPS): a rapid response statement from a committee on behalf of the Board of the International Society for Prenatal Diagnosis, 24 October 2011.Prenatal diagnosis of hypoplastic left heart syndrome and trisomy 18 in a fetus with normal nuchal translucency and abnormal ductus venosus blood flow at 13 weeks of gestation.The ductus venosus in early pregnancy and congenital anomalies.Promises and pitfalls of first trimester sonographic markers in the detection of fetal aneuploidy.Clinical value of the 11- to 13+6-week sonogram for detection of congenital malformations: a review.The CUSUM test applied in prospective nuchal translucency quality review.Heterotrisomy recurrence risk: a practical maternal age-dependent approach for excess trisomy 21 risk calculation after a previous autosomal trisomy.Position statement from the Chromosome Abnormality Screening Committee on behalf of the Board of the International Society for Prenatal Diagnosis.Maternal plasma DNA testing for aneuploidy in pregnancies achieved by assisted reproductive technologies.Adding ductus venosus blood flow as a categorical variable to the Combined and Integrated tests in Down's syndrome screening.First-trimester Down syndrome screening in renal-transplanted pregnant women: a model for adjusting the false-positives rates.Clinical application of midtrimester non-invasive fetal RHD genotyping and identification of RHD variants in a mixed-ethnic population.Birth defects in medically assisted reproduction pregnancies in the city of Barcelona.Prenatal diagnosis in human immunodeficiency virus-infected women: a new screening program for chromosomal anomalies.Response to "On gestational weeks and maths".Combining fetal nuchal fold thickness with second-trimester biochemistry to screen for trisomy 21.Increasing detection rates of birth defects by prenatal ultrasound leading to apparent increasing prevalence. Lessons learned from the population-based registry of birth defects of Barcelona.Added value of Chromosomal Microarray Analysis (CMA) over karyotyping in Early Pregnancy Loss - a Systematic Review and Meta-Analysis.Intertwin crown-rump length discordance in the prediction of fetal anomalies, fetal loss and adverse perinatal outcome.Counting ovarian antral follicles by ultrasound: a practical guide.Crown-rump length audit plots with the use of operator-specific PAPP-A and β-hCG median MoM.Maternal IgM antibody status in confirmed fetal cytomegalovirus infection detected by sonographic signs.Antral follicle count as a marker of ovarian biological age to reflect the background risk of fetal aneuploidy.The effect of maternal age on chromosomal anomaly rate and spectrum in recurrent miscarriage.Parental Origin of the Retained X Chromosome in Monosomy X Miscarriages and Ongoing Pregnancies.Likelihood ratios to apply for nasal bone, ductus venosus and tricuspid flow at the 11-13 weeks' scan in down syndrome screening.Fragile X syndrome prenatal diagnosis: parental attitudes and reproductive responses.Increased nuchal translucency and normal karyotype: perinatal and pediatric outcomes at 2 years of age.Aneuploidy screening: a position statement from a committee on behalf of the Board of the International Society for Prenatal Diagnosis, January 2011.A new comprehensive paradigm for Prenatal Diagnosis.Reliability analysis on ductus venosus assessment at 11-14 weeks' gestation in a high-risk population.Cisterna magna width at 11-13 weeks in the detection of posterior fossa anomalies.Updated reference ranges for the ductus venosus pulsatility index at 11-13 weeks.Genomic Microarray in Fetuses with Early Growth Restriction: A Multicenter Study.Fetal heart rate patterns in pregnancies with chromosomal disorders or subsequent fetal loss.Infección congénita por citomegalovirus con una afección ecográfica progresiva y graveRapid fetal karyotype from cystic hygroma and pleural effusions
P50
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P50
description
hulumtues
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onderzoeker
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researcher
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ricercatore
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հետազոտող
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name
Antoni Borrell
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Antoni Borrell
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Antoni Borrell
@es
Antoni Borrell
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Antoni Borrell
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type
label
Antoni Borrell
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Antoni Borrell
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Antoni Borrell
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Antoni Borrell
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Antoni Borrell
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prefLabel
Antoni Borrell
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Antoni Borrell
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Antoni Borrell
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Antoni Borrell
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Antoni Borrell
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P214
P106
P1153
7004925436
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P21
P214
P31
P496
0000-0002-4304-4797
P569
2000-01-01T00:00:00Z
P735
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viaf-305878520