Incidence of non-age-dependent chromosomal abnormalities: a population-based study on 88965 amniocenteses.
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Non-Invasive Prenatal Testing Using Cell Free DNA in Maternal Plasma: Recent Developments and Future ProspectsFetal Cell Based Prenatal Diagnosis: Perspectives on the Present and FutureMALDI-TOF MS in Prenatal Genomics.Non-invasive prenatal chromosomal aneuploidy testing--clinical experience: 100,000 clinical samples.Noninvasive prenatal screening for fetal aneuploidy, 2016 update: a position statement of the American College of Medical Genetics and Genomics.Clinical diagnostic testing for the cytogenetic and molecular causes of male infertility: the Mayo Clinic experience.Rare chromosome abnormalities, prevalence and prenatal diagnosis rates from population-based congenital anomaly registers in EuropeGain of FAM123B and ARHGEF9 in an Obese Man with Intellectual Disability, Congenital Heart Defects and Multiple Supernumerary Ring Chromosomes.Karyotype analysis in large-sample infertile couples living in Central China: a study of 14965 couples.Should advanced maternal age be a reasonable indication for invasive diagnostic testing?Enlarged NT (≥3.5 mm) in the first trimester - not all chromosome aberrations can be detected by NIPT.Delayed childbearing: effects on fertility and the outcome of pregnancy.ACMG statement on noninvasive prenatal screening for fetal aneuploidy.Non-invasive prenatal testing for aneuploidy: current status and future prospects.What does next-generation sequencing mean for prenatal diagnosis?Chromosomal polymorphism in mammals: an evolutionary perspective.Expanding non-invasive prenatal testing beyond chromosomes 21, 18, 13, X and Y.Only a minority of sex chromosome abnormalities are detected by a national prenatal screening program for Down syndrome.Ultrastructural and cytogenetic analyses of mature human oocyte dysmorphisms with respect to clinical outcomes.Chromosome abnormalities diagnosed in utero: a Japanese study of 28 983 amniotic fluid specimens collected before 22 weeks gestations.Pathologic ultrasound findings and risk for congenital anomalies in teenage pregnancies.Genomic Investigation of Balanced Chromosomal Rearrangements in Patients with Abnormal Phenotypes.Clinical accuracy of abnormal cell-free fetal DNA results for the sex chromosomes.Fetal axillary cystic hygroma: a novel association with triple X syndrome.Structural chromosomal abnormalities detected during CVS analysis and their role in the prenatal ascertainment of cryptic subtelomeric rearrangements
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P2860
Incidence of non-age-dependent chromosomal abnormalities: a population-based study on 88965 amniocenteses.
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2009 nî lūn-bûn
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2009 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2009年の論文
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2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
name
Incidence of non-age-dependent ...... study on 88965 amniocenteses.
@ast
Incidence of non-age-dependent ...... study on 88965 amniocenteses.
@en
Incidence of non-age-dependent ...... study on 88965 amniocenteses.
@nl
type
label
Incidence of non-age-dependent ...... study on 88965 amniocenteses.
@ast
Incidence of non-age-dependent ...... study on 88965 amniocenteses.
@en
Incidence of non-age-dependent ...... study on 88965 amniocenteses.
@nl
prefLabel
Incidence of non-age-dependent ...... study on 88965 amniocenteses.
@ast
Incidence of non-age-dependent ...... study on 88965 amniocenteses.
@en
Incidence of non-age-dependent ...... study on 88965 amniocenteses.
@nl
P2860
P356
P1476
Incidence of non-age-dependent ...... d study on 88965 amniocenteses
@en
P2093
Antonino Forabosco
Sandra Santucci
P2860
P2888
P304
P356
10.1038/EJHG.2008.265
P577
2009-01-21T00:00:00Z