The clinical utility of microarray technologies applied to prenatal cytogenetics in the presence of a normal conventional karyotype: a review of the literature.
about
Prevalence of recurrent pathogenic microdeletions and microduplications in over 9500 pregnanciesAn exploration of genetic counselors' needs and experiences with prenatal chromosomal microarray testingPromises, pitfalls and practicalities of prenatal whole exome sequencing.Whole-genome array CGH evaluation for replacing prenatal karyotyping in Hong KongCopy number variants, aneuploidies, and human diseaseClinical utility of array comparative genomic hybridisation in prenatal setting.Limited Clinical Utility of Non-invasive Prenatal Testing for Subchromosomal Abnormalities.Chromosomal Microarrays in Prenatal Diagnosis: Time for a Change of Policy?Prenatal diagnosis of chromosomal imbalances.Exome sequencing for gene discovery in lethal fetal disorders--harnessing the value of extreme phenotypes.Genomic futures of prenatal screening: ethical reflection.Microarray Technology for the Diagnosis of Fetal Chromosomal Aberrations: Which Platform Should We Use?Prenatal diagnosis of congenital upper limb differences: a current concept review.Cell-free fetal DNA: the new tool in fetal medicineACOG and SMFM guidelines for prenatal diagnosis: Is karyotyping really sufficient?Challenges in non-invasive prenatal screening for sub-chromosomal copy number variations using cell-free DNA.Cut-off value of nuchal translucency as indication for chromosomal microarray analysis.Prenatal diagnosis by chromosomal microarray analysis.Prenatal screening for genetic disorders: Suggested guidelines for the Indian Scenario.Prenatal diagnosis of submicroscopic chromosomal aberrations in fetuses with ventricular septal defects by chromosomal microarray-based analysis.Practice guideline: joint CCMG-SOGC recommendations for the use of chromosomal microarray analysis for prenatal diagnosis and assessment of fetal loss in Canada.Current controversies in prenatal diagnosis 2: should a fetal exome be used in the assessment of a dysmorphic or malformed fetus?Exome sequencing for prenatal diagnosis of fetuses with sonographic abnormalities
P2860
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P2860
The clinical utility of microarray technologies applied to prenatal cytogenetics in the presence of a normal conventional karyotype: a review of the literature.
description
2013 nî lūn-bûn
@nan
2013 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2013 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2013年の論文
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2013年学术文章
@wuu
2013年学术文章
@zh-cn
2013年学术文章
@zh-hans
2013年学术文章
@zh-my
2013年学术文章
@zh-sg
2013年學術文章
@yue
name
The clinical utility of microa ...... e: a review of the literature.
@ast
The clinical utility of microa ...... e: a review of the literature.
@en
The clinical utility of microa ...... e: a review of the literature.
@nl
type
label
The clinical utility of microa ...... e: a review of the literature.
@ast
The clinical utility of microa ...... e: a review of the literature.
@en
The clinical utility of microa ...... e: a review of the literature.
@nl
prefLabel
The clinical utility of microa ...... e: a review of the literature.
@ast
The clinical utility of microa ...... e: a review of the literature.
@en
The clinical utility of microa ...... e: a review of the literature.
@nl
P2093
P2860
P356
P1433
P1476
The clinical utility of microa ...... e: a review of the literature.
@en
P2093
Jill A Rosenfeld
John A Crolla
Jonathan L A Callaway
Lisa G Shaffer
P2860
P304
P356
10.1002/PD.4209
P50
P577
2013-09-08T00:00:00Z
2013-12-01T00:00:00Z