(Q33910274)

English

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

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scholarly article

1 reference

Europe PubMed Central

30 July 2017

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

1 reference

Europe PubMed Central

30 July 2017

0 references

Christa Lese Martin

6

object named as

Christa Lese Martin

1 reference

Europe PubMed Central

30 July 2017

David H. Ledbetter

5

object named as

David H Ledbetter

1 reference

Europe PubMed Central

30 July 2017

author name string

Anthony J Schaeffer

1

1 reference

Europe PubMed Central

30 July 2017

June Chung

2

1 reference

Europe PubMed Central

30 July 2017

Konstantina Heretis

3

1 reference

Europe PubMed Central

30 July 2017

Andrew Wong

4

1 reference

Europe PubMed Central

30 July 2017

language of work or name

0 references

publication date

4 May 2004

1 reference

Europe PubMed Central

30 July 2017

American Journal of Human Genetics

1 reference

Europe PubMed Central

30 July 2017

74

1 reference

Europe PubMed Central

30 July 2017

1168-1174

1 reference

Europe PubMed Central

30 July 2017

6

1 reference

Europe PubMed Central

30 July 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182080

5 July 2018

Genomic microarrays in human genetic disease and cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182080

5 July 2018

DNA microarray analysis in malignant lymphomas.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182080

5 July 2018

High-resolution analysis of paraffin-embedded and formalin-fixed prostate tumors using comparative genomic hybridization to genomic microarrays

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182080

5 July 2018

High-throughput analysis of subtelomeric chromosome rearrangements by use of 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=1182080

5 July 2018

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=1182080

5 July 2018

Diagnosis of aneuploidy in archival, paraffin-embedded pregnancy-loss tissues by comparative genomic hybridization.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182080

5 July 2018

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=1182080

5 July 2018

Cytogenetic diagnosis of "normal 46,XX" karyotypes in spontaneous abortions frequently may be misleading

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182080

5 July 2018

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=1182080

5 July 2018

Autism or atypical autism in maternally but not paternally derived proximal 15q duplication

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182080

5 July 2018

Comparative genomic hybridization for molecular cytogenetic analysis of solid tumors

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182080

5 July 2018

Genome scanning with array CGH delineates regional alterations in mouse islet carcinomas

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182080

29 October 2018

High resolution comparative genomic hybridisation in clinical cytogenetics

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182080

29 October 2018

Genetic aspects of miscarriage

1 reference

https://pubmed.ncbi.nlm.nih.gov/15127362

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Detection of chromosomal aberration in fetuses arising from recurrent spontaneous abortion by comparative genomic hybridization

1 reference

https://pubmed.ncbi.nlm.nih.gov/15127362

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A cytogenetic study of 1000 spontaneous abortions

1 reference

https://pubmed.ncbi.nlm.nih.gov/15127362

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ring 21 chromosome and a satellited 1p in the same patient: novel origin for an ectopic NOR

1 reference

https://pubmed.ncbi.nlm.nih.gov/15127362

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular characterization of a patient with central nervous system dysmyelination and cryptic unbalanced translocation between chromosomes 4q and 18q

1 reference

https://pubmed.ncbi.nlm.nih.gov/15127362

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genome-wide detection of chromosomal imbalances in tumors using BAC microarrays

1 reference

https://pubmed.ncbi.nlm.nih.gov/15127362

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cytogenetic analysis of trophoblasts by comparative genomic hybridization in embryo-fetal development anomalies

1 reference

https://pubmed.ncbi.nlm.nih.gov/15127362

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cytogenetic analyses of culture failures by comparative genomic hybridisation (CGH)-Re-evaluation of chromosome aberration rates in early spontaneous abortions

1 reference

https://pubmed.ncbi.nlm.nih.gov/15127362

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

1 reference

Europe PubMed Central

30 July 2017

1 reference

Europe PubMed Central

30 July 2017

1 reference

Europe PubMed Central

30 July 2017

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