Neural tube defects in the sample of genetic counsellingCornelia de Lange syndrome (CdLS): prenatal and autopsy findingsDetection rates of clinically significant genomic alterations by microarray analysis for specific anomalies detected by ultrasoundSNP-based non-invasive prenatal testing detects sex chromosome aneuploidies with high accuracyNoninvasive prenatal aneuploidy testing of chromosomes 13, 18, 21, X, and Y, using targeted sequencing of polymorphic lociBarth syndrome: an X-linked cause of fetal cardiomyopathy and stillbirthFounder Fukutin mutation causes Walker-Warburg syndrome in four Ashkenazi Jewish familiesFirst-trimester intrauterine Zika virus infection and brain pathology: prenatal and postnatal neuroimaging findingsAssociated ultrasonographic findings in fetuses with microcephaly due to suspected Zika virus (ZIKV) infection during pregnancyComputer-assisted surgical planning and intraoperative guidance in fetal surgery: a systematic reviewTreatment of poor placentation and the prevention of associated adverse outcomes--what does the future hold?Fetal surgery in complicated monoamniotic pregnancies: case series and systematic review of the literatureImaging of congenital Zika virus infection: the route to identification of prognostic factorsDo recent US Supreme Court rulings on patenting of genes and genetic diagnostics affect the practice of genetic screening and diagnosis in prenatal and reproductive care?Fetoplacental chromosomal discrepancyFetal demise with Smith-Lemli-Opitz syndrome confirmed by tissue sterol analysis and the absence of measurable 7-dehydrocholesterol Delta(7)-reductase activity in chorionic villiRevised guidelines for the diagnosis of mosaicism in amniocytesCytogenetic aspects of the Canadian early and mid-trimester amniotic fluid trial (CEMAT)Common trisomy mosaicism diagnosed in amniocytes involving chromosomes 13, 18, 20 and 21: karyotype-phenotype correlationsPrenatal diagnosis of sanfilippo type A syndrome in a family with S66W mutant alleleThe predictive value of findings of the common aneuploidies, trisomies 13, 18 and 21, and numerical sex chromosome abnormalities at CVS: experience from the ACC U.K. Collaborative Study. Association of Clinical Cytogeneticists Prenatal Diagnosis WorFirst-trimester screening for Down syndrome in France combining fetal nuchal translucency measurement and biochemical markersEmbryonic and fetal globins are expressed in adult erythroid progenitor cells and in erythroid cell culturesMolecular diagnosis of a novel heterozygous 268C-->T (R90C) mutation in TGIF gene in a fetus with holoprosencephaly and premaxillary agenesisRaised maternal serum placenta growth factor concentration during the second trimester is associated with Down syndromeRare trisomy mosaicism diagnosed in amniocytes, involving an autosome other than chromosomes 13, 18, 20, and 21: karyotype/phenotype correlationsPostnatal follow-up of prenatally diagnosed trisomy 16 mosaicismPrenatal diagnosis of free sialic acid storage disorders (SASD)Confined placental mosaicism, IUGR, and adverse pregnancy outcome: a controlled retrospective U.K. collaborative surveyAbnormal Shh and FOXC2 expression correlates with aberrant lymphatic development in human fetuses with increased nuchal translucencyAccuracy of cytogenetic findings on chorionic villus sampling (CVS)--diagnostic consequences of CVS mosaicism and non-mosaic discrepancy in centres contributing to EUCROMIC 1986-1992Genetic considerations in the prenatal diagnosis of overgrowth syndromesMillions of missing girls: from fetal sexing to high technology sex selection in IndiaProspective audit of a one-centre combined nuchal translucency and triple test programme for the detection of trisomy 21Prevalence of recurrent pathogenic microdeletions and microduplications in over 9500 pregnanciesPrenatal diagnosis of 'isolated' Dandy-Walker malformation: imaging findings and prenatal counsellingFollow-up of pregnancies complicated by placental mosaicism diagnosed by chorionic villus samplingProspective prenatal investigations on potential uniparental disomy in cases of confined placental trisomyEuropean collaborative study on prenatal diagnosis: mosaicism, pseudomosaicism and single abnormal cells in amniotic fluid cell culturesFirst-trimester screening for trisomy 21 combining biochemistry and ultrasound at individually optimal gestational ages. An interventional study
P1433
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P1433
description
journal
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revista científica
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rivista scientifica
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wetenschappelijk tijdschrift van Wiley-Blackwell
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wissenschaftliche Fachzeitschrift
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مجلة
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Prenatal Diagnosis
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Prenatal Diagnosis
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Prenatal Diagnosis
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Prenatal Diagnosis
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Prenatal Diagnosis
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Prenatal Diagnosis
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Prenatal Diagnosis
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Prenatal Diagnosis
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Prenatal Diagnosis
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Prenatal Diagnosis
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Prenatal Diagnosis
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Prenatal Diagnosis
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Prenatal Diagnosis
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Prenatal Diagnosis
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Prenatal Diagnosis
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Prenatal Diagnosis
@fi
Prenatal Diagnosis
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Prenatal Diagnosis
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Prenatal Diagnosis
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Prenatal Diagnosis
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prefLabel
Prenatal Diagnosis
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Prenatal Diagnosis
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Prenatal Diagnosis
@de
Prenatal Diagnosis
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Prenatal Diagnosis
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Prenatal Diagnosis
@fi
Prenatal Diagnosis
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Prenatal Diagnosis
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Prenatal Diagnosis
@nb
Prenatal Diagnosis
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P31
P3181
P1055
P1058
P1156
P123
P1277
P1476
Prenatal Diagnosis
@und
P236
P571
1981-01-01T00:00:00Z