(Q51577633)

English

Identification of origin of unknown derivative chromosomes by array-based comparative genomic hybridization using pre- and postnatal clinical samples.

scientific article published on 17 October 2007

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scholarly article

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17940726%20AND%20SRC:MED&resulttype=core&format=json

8 January 2020

Identification of origin of unknown derivative chromosomes by array-based comparative genomic hybridization using pre- and postnatal clinical samples (English)

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17940726%20AND%20SRC:MED&resulttype=core&format=json

8 January 2020

2

1 reference

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8 January 2020

author name string

Jin Choe

1

1 reference

Europe PubMed Central

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8 January 2020

Chang-Jun Bae

3

1 reference

Europe PubMed Central

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8 January 2020

Dong-Suk Lee

4

1 reference

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8 January 2020

Doyeong Hwang

5

1 reference

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8 January 2020

Ki-Chul Kim

6

1 reference

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8 January 2020

Woong-Yang Park

7

1 reference

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8 January 2020

Jong-Ho Lee

8

1 reference

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8 January 2020

Jeong-Sun Seo

9

1 reference

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8 January 2020

publication date

17 October 2007

1 reference

Europe PubMed Central

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8 January 2020

Journal of Human Genetics

1 reference

Europe PubMed Central

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8 January 2020

52

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8 January 2020

11

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8 January 2020

934-942

1 reference

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8 January 2020

https://scigraph.springernature.com/pub.10.1007/s10038-007-0199-1

0 references

DNA copy-number analysis of the 22q11 deletion-syndrome region using array-CGH with genomic and PCR-based targets.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17940726

12 December 2020

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Small supernumerary marker chromosomes – progress towards a genotype-phenotype correlation

1 reference

https://pubmed.ncbi.nlm.nih.gov/17940726

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Characterisation of supernumerary chromosomal markers: a study of 13 cases

1 reference

https://pubmed.ncbi.nlm.nih.gov/17940726

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A cytogeneticist's perspective on genomic microarrays

1 reference

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Molecular mechanisms for constitutional chromosomal rearrangements in humans

1 reference

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Klinefelter's syndrome as a model of anomalous cerebral laterality: testing gene dosage in the X chromosome pseudoautosomal region using a DNA microarray.

1 reference

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Chemical differentiation along metaphase chromosomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/17940726

12 December 2020

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Small supernumerary marker chromosomes (sSMC) in humans

1 reference

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12 December 2020

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Development and validation of a CGH microarray for clinical cytogenetic diagnosis

1 reference

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

1 reference

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A tiling resolution DNA microarray with complete coverage of the human genome

1 reference

https://pubmed.ncbi.nlm.nih.gov/17940726

12 December 2020

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/17940726

12 December 2020

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Quantitative mapping of amplicon structure by array CGH identifies CYP24 as a candidate oncogene

1 reference

https://pubmed.ncbi.nlm.nih.gov/17940726

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prenatal detection of unbalanced chromosomal rearrangements by array CGH.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17940726

12 December 2020

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Cytogenetic analysis using quantitative, high-sensitivity, fluorescence hybridization

1 reference

https://pubmed.ncbi.nlm.nih.gov/17940726

12 December 2020

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inferred from PubMed ID database lookup

Molecular karyotyping: array CGH quality criteria for constitutional genetic diagnosis.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17940726

12 December 2020

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High resolution deletion analysis of constitutional DNA from neurofibromatosis type 2 (NF2) patients using microarray-CGH

1 reference

https://pubmed.ncbi.nlm.nih.gov/17940726

12 December 2020

based on heuristic

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Two new cases ofde novo small supernumerary marker chromosomes (sSMC) detected at prenatal diagnosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/17940726

12 December 2020

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Matrix-based comparative genomic hybridization: biochips to screen for genomic imbalances

1 reference

https://pubmed.ncbi.nlm.nih.gov/17940726

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/17940726

12 December 2020

based on heuristic

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Representational oligonucleotide microarray analysis: a high-resolution method to detect genome copy number variation

1 reference

https://pubmed.ncbi.nlm.nih.gov/17940726

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prenatal detection and characterization of a small supernumerary marker chromosome (sSMC) derived from chromosome 22 with apparently normal phenotype

1 reference

https://pubmed.ncbi.nlm.nih.gov/17940726

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Large-scale copy number polymorphism in the human genome

1 reference

https://pubmed.ncbi.nlm.nih.gov/17940726

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Microarray comparative genomic hybridization (CGH)-based prenatal diagnosis for chromosome abnormalities using cell-free fetal DNA in amniotic fluid

1 reference

https://pubmed.ncbi.nlm.nih.gov/17940726

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Y chromosome loss and other genomic alterations in hepatocellular carcinoma cell lines analyzed by CGH and CGH array

1 reference

https://pubmed.ncbi.nlm.nih.gov/17940726

12 December 2020

based on heuristic

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Detection of cryptic chromosome aberrations in a patient with a balanced t(1;9)(p34.2;p24) by array-based comparative genomic hybridization.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17940726

12 December 2020

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Development of a comparative genomic hybridization microarray and demonstration of its utility with 25 well-characterized 1p36 deletions.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17940726

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Array comparative genomic hybridization analysis of uterine leiomyosarcoma.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17940726

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prenatal diagnosis of chromosomal abnormalities using array-based comparative genomic hybridization

1 reference

https://pubmed.ncbi.nlm.nih.gov/17940726

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/17940726

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/17940726

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/17940726

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Targeted genomic microarray analysis for identification of chromosome abnormalities in 1500 consecutive clinical cases.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17940726

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Detection of large-scale variation in the human genome

1 reference

https://pubmed.ncbi.nlm.nih.gov/17940726

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