(Q37938895)

25 August 2017

3 references

19 September 2019

12 October 2019

23 July 2020

Chromosome analysis using spectral karyotyping (SKY). (English)

1 reference

biomedical investigative technique

25 August 2017

0 references

1 reference

19 September 2019

1 reference

12 October 2019

1 reference

23 July 2020

George Imataka

1

1 reference

PMCID

3254861

25 August 2017

Osamu Arisaka

series ordinal

2

1 reference

25 August 2017

1 January 2012

4 references

Cell Biochemistry and Biophysics

25 August 2017

19 September 2019

12 October 2019

23 July 2020

4 references

25 August 2017

19 September 2019

12 October 2019

23 July 2020

62

1 reference

25 August 2017

1

1 reference

25 August 2017

13-17

1 reference

https://scigraph.springernature.com/pub.10.1007/s12013-011-9285-2

25 August 2017

0 references

cites work

Multiple congenital anomaly caused by an extra autosome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3254861

Chromosome studies on normal and leukemic human leukocytes

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3254861

6 September 2017

A new trisomic syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3254861

Chromosome preparations of leukocytes cultured from human peripheral blood

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3254861

Mongolism; a chromosomal disease (trisomy).

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3254861

A sex-chromosome anomaly in a case of gonadal dysgenesis (Turner's syndrome).

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3254861

Multicolor Spectral Karyotyping of Human Chromosomes

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3254861

The 13q-deletion syndrome

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3254861

The human genome project: past, present, and future

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3254861

Fluorescence in situ hybridization: applications in cytogenetics and gene mapping

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3254861

Comparative genomic hybridization for molecular cytogenetic analysis of solid tumors

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3254861

High-resolution chromosome analysis in clinical medicine

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3254861

The discovery of the human chromosome number in Lund, 1955-1956.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3254861

An analysis of epilepsy with chromosomal abnormalities

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3254861

Study by fluorescence of a trisomy C mosaic, probably 8: 46,XY-47,XY,?8+

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3254861

Trisomy 11/22 diagnosed by spectral karyotyping (SKY)

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3254861

Development of spectral colour banding in cytogenetic analysis

1 October 2018

1 reference

12 December 2020

Survival of trisomy 18 cases in Japan

1 reference

12 December 2020

Automatic karyotyping of quinacrine mustard stained human chromosomes

1 reference

12 December 2020

The 11q;22q translocation: a collaborative study of 20 new cases and analysis of 110 families

1 reference

12 December 2020

Genes on the Y chromosome influencing rate of maturation in man: skeletal age studies in children with Klinefelter's (XXY) and Turner's (XO) syndromes

1 reference

12 December 2020

Down syndrome with acute epiglottitis

1 reference

12 December 2020

10.1007/S12013-011-9285-2

Identifiers

DOI

1 reference

25 August 2017

1 reference

25 August 2017

1 reference

PMCID

3254861