Microarray application in prenatal diagnosis: a position statement from the cytogenetics working group of the Italian Society of Human Genetics (SIGU), November 2011
about
Microarray comparative genomic hybridization in prenatal diagnosis: a reviewRecent advances in the prenatal interrogation of the human fetal genome.The future of prenatal diagnosis: karyotype, microarray or both? Technical and ethical considerations.Whole-genome array CGH evaluation for replacing prenatal karyotyping in Hong KongPrenatal Diagnosis of Chromosome Abnormalities: A 13-Year Institution Experience.Noninvasive detection of fetal subchromosome abnormalities via deep sequencing of maternal plasma.Karyotype analysis in large-sample infertile couples living in Central China: a study of 14965 couples.Chromosomal Microarrays in Prenatal Diagnosis: Time for a Change of Policy?What results to disclose, when, and who decides? Healthcare professionals' views on prenatal chromosomal microarray analysis.Women's experiences receiving abnormal prenatal chromosomal microarray testing results.Chromosomal microarray analysis as a first-tier clinical diagnostic test: Estonian experience.Use of prenatal chromosomal microarray: prospective cohort study and systematic review and meta-analysis.A new case of interstitial 1q 25.3-32.1 deletion: cytogenetic analysis molecular characterization and ultrasound findings.High-resolution chromosomal microarrays in prenatal diagnosis significantly increase diagnostic power.Prenatal microarray analysis as second-tier diagnostic test: single-center prospective study.Prenatal diagnosis of chromosomal abnormalities in fetuses with abnormal cardiac ultrasound findings: evaluation of chromosomal microarray-based analysis.The clinical utility and indications of chromosomal microarray analysis in prenatal diagnosis.Prenatal diagnosis using combined quantitative fluorescent polymerase chain reaction and array comparative genomic hybridization analysis as a first-line test: results from over 1000 consecutive cases.408 kb 15q11.2 microduplication by array comparative genomic hybridization in a fetus presenting with exomphalos, micrognathia, tetralogy of Fallot and normal karyotype: a genetic counseling dilemma in paternal carrier status.Prenatal diagnosis of chromosomal mosaicism in over 1600 cases using array comparative genomic hybridization as a first line test.Practice guideline: joint CCMG-SOGC recommendations for the use of chromosomal microarray analysis for prenatal diagnosis and assessment of fetal loss in Canada.
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P2860
Microarray application in prenatal diagnosis: a position statement from the cytogenetics working group of the Italian Society of Human Genetics (SIGU), November 2011
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2012 թուականի Ապրիլին հրատարակուած գիտական յօդուած
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2012 թվականի ապրիլին հրատարակված գիտական հոդված
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2012年の論文
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2012年論文
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2012年論文
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2012年論文
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2012年論文
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2012年論文
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2012年论文
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name
Microarray application in pren ...... Genetics (SIGU), November 2011
@ast
Microarray application in pren ...... Genetics (SIGU), November 2011
@en
Microarray application in pren ...... Genetics (SIGU), November 2011
@nl
type
label
Microarray application in pren ...... Genetics (SIGU), November 2011
@ast
Microarray application in pren ...... Genetics (SIGU), November 2011
@en
Microarray application in pren ...... Genetics (SIGU), November 2011
@nl
prefLabel
Microarray application in pren ...... Genetics (SIGU), November 2011
@ast
Microarray application in pren ...... Genetics (SIGU), November 2011
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Microarray application in pren ...... Genetics (SIGU), November 2011
@nl
P2093
P2860
P356
P1476
Microarray application in pren ...... Genetics (SIGU), November 2011
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P2093
A. M. Nardone
A. Novelli
D. Bizzoco
D. Giardino
F. R. Grati
L. Ballarati
L. Bernardini
L. Camurri
P2860
P356
10.1002/UOG.11092
P407
P577
2012-04-01T00:00:00Z