Genome-wide array-based copy number profiling in human placentas from unexplained stillbirths - Wikidata - wikimedia - TriplyDB

Genome-wide array-based copy number profiling in human placentas from unexplained stillbirths

Genome-wide array-based copy number profiling in human placentas from unexplained stillbirths

http://www.wikidata.org/entity/Q35242256

about

From prenatal genomic diagnosis to fetal personalized medicine: progress and challenges.Structural genomic variation as risk factor for idiopathic recurrent miscarriage.Karyotype versus microarray testing for genetic abnormalities after stillbirth.A robust approach for blind detection of balanced chromosomal rearrangements with whole-genome low-coverage sequencing.Extensive load of somatic CNVs in the human placenta.Rescue karyotyping: a case series of array-based comparative genomic hybridization evaluation of archival conceptual tissue.Meta-analysis of morphometric parameters of late-gestation fetal sheep developed under natural and artificial constraints.Diagnostic utility of microarray testing in pregnancy loss.The role of DNA microarrays in the evaluation of fetal death.

P2860

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P2860

Genome-wide array-based copy number profiling in human placentas from unexplained stillbirths

http://www.wikidata.org/entity/Q35242256

description

2011 nî lūn-bûn

@nan

2011 թուականի Յուլիսին հրատարակուած գիտական յօդուած

@hyw

2011 թվականի հուլիսին հրատարակված գիտական հոդված

@hy

2011年の論文

@ja

2011年論文

@yue

2011年論文

@zh-hant

2011年論文

@zh-hk

2011年論文

@zh-mo

2011年論文

@zh-tw

2011年论文

@wuu

name

Genome-wide array-based copy n ...... s from unexplained stillbirths

@ast

Genome-wide array-based copy n ...... s from unexplained stillbirths

@en

type

label

Genome-wide array-based copy n ...... s from unexplained stillbirths

@ast

Genome-wide array-based copy n ...... s from unexplained stillbirths

@en

prefLabel

Genome-wide array-based copy n ...... s from unexplained stillbirths

@ast

Genome-wide array-based copy n ...... s from unexplained stillbirths

@en

P1433

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P1433

Prenatal Diagnosis

P1476

Genome-wide array-based copy n ...... s from unexplained stillbirths

@en

P2093

Francesca Ferrari

http://www.w3.org/2001/XMLSchema#string

Ignatia Van Den Veyver

http://www.w3.org/2001/XMLSchema#string

Kjersti Aagaard-Tillery

http://www.w3.org/2001/XMLSchema#string

R Alan Harris

http://www.w3.org/2001/XMLSchema#string

Shay Ben-Shachar

http://www.w3.org/2001/XMLSchema#string

Xiaoling Wang

http://www.w3.org/2001/XMLSchema#string

P2860

Strong association of de novo copy number mutations with autism

Global variation in copy number in the human genome

A common inversion under selection in Europeans

Copy number variants and common disorders: filling the gaps and exploring complexity in genome-wide association studies.

Array comparative genomic hybridization and flow cytometry analysis of spontaneous abortions and mors in utero samples.

Array-based comparative genomic hybridization for the genomewide detection of submicroscopic chromosomal abnormalities.

Comparative genomic hybridization-array analysis enhances the detection of aneuploidies and submicroscopic imbalances in spontaneous miscarriages

Classification of stillbirth by relevant condition at death (ReCoDe): population based cohort study

Prenatal diagnosis by array-CGH.

P304

932-944

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

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10.1002/PD.2817

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10

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31

http://www.w3.org/2001/XMLSchema#string

P50

Fabio Facchinetti

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2011-07-05T00:00:00Z

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51470408

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21732394

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P932

3183137

http://www.w3.org/2001/XMLSchema#string