(Q36369737)

English

Array-based comparative genomic hybridization is more informative than conventional karyotyping and fluorescence in situ hybridization in the analysis of first-trimester spontaneous abortion

scientific article

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

Array-based comparative genomic hybridization is more informative than conventional karyotyping and fluorescence in situ hybridization in the analysis of first-trimester spontaneous abortion (English)

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

0 references

0 references

1

object named as

Jinsong Gao

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

9

object named as

Xuming Bian

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

author name string

Congcong Liu

2

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

Fengxia Yao

3

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

Na Hao

4

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

Jing Zhou

5

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

Qian Zhou

6

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

Liang Zhang

7

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

Xinyan Liu

8

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

Juntao Liu

10

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

publication date

16 July 2012

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

Molecular Cytogenetics

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

5

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

1

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

33

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

Additional information from array comparative genomic hybridization technology over conventional karyotyping in prenatal diagnosis: a systematic review and meta-analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3488553

30 September 2017

Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3488553

30 September 2017

Preprocessing and downstream analysis of microarray DNA copy number profiles

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3488553

30 September 2017

Genome-wide oligonucleotide array comparative genomic hybridization for etiological diagnosis of mental retardation: a multicenter experience of 1499 clinical cases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3488553

30 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3488553

30 September 2017

Diagnosis of miscarriages by molecular karyotyping: benefits and pitfalls

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3488553

30 September 2017

Detecting sex chromosome anomalies and common triploidies in products of conception by array-based comparative genomic hybridization

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3488553

30 September 2017

Will the new cytogenetics replace the old cytogenetics?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3488553

30 September 2017

Chromosome abnormalities identified in 347 spontaneous abortions collected in Japan

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3488553

30 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3488553

30 September 2017

Rapid and simple prenatal diagnosis of common chromosome disorders: advantages and disadvantages of the molecular methods FISH and QF-PCR.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3488553

30 September 2017

Assembly of microarrays for genome-wide measurement of DNA copy number

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3488553

30 September 2017

Comparative genomic hybridization in combination with flow cytometry improves results of cytogenetic analysis of spontaneous abortions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3488553

30 September 2017

Genome-wide analysis of DNA copy-number changes using cDNA microarrays

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3488553

30 September 2017

High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3488553

30 September 2017

Prenatal detection of chromosome aneuploidies in uncultured chorionic villus samples by FISH

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3488553

30 September 2017

Estimates of human fertility and pregnancy loss.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3488553

30 September 2017

Clinical utility of array comparative genomic hybridisation for prenatal diagnosis: a cohort study of 3171 pregnancies.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3488553

21 September 2018

Genomic changes detected by array CGH in human embryos with developmental defects

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3488553

21 September 2018

Array comparative genomic hybridization profiling of first-trimester spontaneous abortions that fail to grow in vitro.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3488553

21 September 2018

Prenatal detection of chromosome aneuploidies by fluorescence in situ hybridization: experience with 2000 uncultured amniotic fluid samples in a prospective preclinical trial.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3488553

21 September 2018

Identification of copy number variants in miscarriages from couples with idiopathic recurrent pregnancy loss

1 reference

https://api.crossref.org/works/10.1186%2F1755-8166-5-33

21 January 2018

Application of quantitative fluorescent PCR with short tandem repeat markers to the study of aneuploidies in spontaneous miscarriages

1 reference

https://pubmed.ncbi.nlm.nih.gov/22794168

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Array comparative genomic hybridization analysis in first-trimester spontaneous abortions with 'normal' karyotypes

1 reference

https://pubmed.ncbi.nlm.nih.gov/22794168

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic analysis of first-trimester miscarriages with a combination of cytogenetic karyotyping, microsatellite genotyping and arrayCGH

1 reference

https://pubmed.ncbi.nlm.nih.gov/22794168

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Multiplex interphase FISH as a screen for common aneuploidies in spontaneous abortions

1 reference

https://pubmed.ncbi.nlm.nih.gov/22794168

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Rapid prenatal diagnostics in the interphase nucleus: procedure and cut-off rates

1 reference

https://pubmed.ncbi.nlm.nih.gov/22794168

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

High-throughput analysis of chromosome abnormality in spontaneous miscarriage using an MLPA subtelomere assay with an ancillary FISH test for polyploidy

1 reference

https://pubmed.ncbi.nlm.nih.gov/22794168

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cytogenetic studies in spontaneous abortion: the Calgary experience

1 reference

https://pubmed.ncbi.nlm.nih.gov/22794168

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic factors in recurrent abortion

1 reference

https://pubmed.ncbi.nlm.nih.gov/22794168

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Collection of villous tissue under ultrasound guidance to improve the cytogenetic study of early pregnancy failure

1 reference

https://pubmed.ncbi.nlm.nih.gov/22794168

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1186/1755-8166-5-33

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

Dimensions Publication ID

0 references

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

ResearchGate publication ID

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q36369737&oldid=2198775390"