(Q41879810)

13 October 2017

The clinical application of array CGH for the detection of chromosomal defects in 20,126 unselected newborns (English)

1 reference

13 October 2017

Sang-Jin Park

1

1 reference

13 October 2017

Eun Hye Jung

2

1 reference

13 October 2017

Ran-Suk Ryu

3

1 reference

13 October 2017

Hyun Woong Kang

4

1 reference

13 October 2017

He Doo Chung

5

1 reference

13 October 2017

Ho-Young Kang

6

1 reference

13 October 2017

language of work or name

1 reference

1 June 2013

1 reference

13 October 2017

Molecular Cytogenetics

1 reference

13 October 2017

6

1 reference

13 October 2017

1

1 reference

13 October 2017

21

1 reference

https://scigraph.springernature.com/pub.10.1186/1755-8166-6-21

13 October 2017

0 references

cites work

Molecular karyotyping by array CGH in a Russian cohort of children with intellectual disability, autism, epilepsy and congenital anomalies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3682880

Genomic disorders on chromosome 22.

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3682880

Down's syndrome and Alzheimer's disease: towards secondary prevention

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3682880

15q11.2 proximal imbalances associated with a diverse array of neuropsychiatric disorders and mild dysmorphic features

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3682880

Experience with microarray-based comparative genomic hybridization for prenatal diagnosis in over 5000 pregnancies

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3682880

Rare chromosome abnormalities, prevalence and prenatal diagnosis rates from population-based congenital anomaly registers in Europe

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3682880

Clinical implementation of whole-genome array CGH as a first-tier test in 5080 pre and postnatal cases

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3682880

The prevalence of congenital anomalies in Europe

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3682880

Sex chromosome trisomies in Europe: prevalence, prenatal detection and outcome of pregnancy

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3682880

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

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3682880

Validation and implementation of array comparative genomic hybridisation as a first line test in place of postnatal karyotyping for genome imbalance.

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3682880

Velo-Cardio-Facial Syndrome

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3682880

A highly annotated whole-genome sequence of a Korean individual

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3682880

New concepts in Klinefelter syndrome

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3682880

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3682880

The schizophrenia phenotype in 22q11 deletion syndrome

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3682880

Is earlier better? At the beginning of schizophrenia: timing and opportunities for early intervention

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3682880

Estimates of the frequency of chromosome abnormalities detectable in unselected newborns using moderate levels of banding

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3682880

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

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3682880

Early recognition of hereditary motor and sensory neuropathy type 1 can avoid life-threatening vincristine neurotoxicity

18 August 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23725218

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

A cytogenetic survey of 14,069 newborn infants. I. Incidence of chromosome abnormalities

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23725218

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Ending the late diagnosis of Turner syndrome through a novel high-throughput assay

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23725218

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1186/1755-8166-6-21

1 reference

13 October 2017

1 reference

13 October 2017

1 reference