(Q34634481)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4646558%20AND%20SRC:MED&resulttype=core&format=json

1 October 2019

title

Ring F chromosome mosaicism (46,XY,20r-46,XY) in an epileptic child without apparent haematological disease (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4646558%20AND%20SRC:MED&resulttype=core&format=json

1 October 2019

main subject

human chromosomes 19-20

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A4646558

16 February 2023

1 reference

16 February 2023

author name string

M. Faed

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A4646558

16 February 2023

H. G. Morton

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A4646558

16 February 2023

J. Robertson

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A4646558

16 February 2023

language of work or name

English

0 references

publication date

1 December 1972

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4646558%20AND%20SRC:MED&resulttype=core&format=json

full work available at URL

1 October 2019

https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/4646558/?tool=EBI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A4646558

https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/4646558/pdf/?tool=EBI

16 February 2023

file format

Portable Document Format

online access status

open access

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A4646558

https://europepmc.org/articles/PMC1469060

16 February 2023

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A4646558

https://europepmc.org/articles/PMC1469060?pdf=render

16 February 2023

file format

Portable Document Format

online access status

open access

content deliverer

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A4646558

https://syndication.highwire.org/content/doi/10.1136/jmg.9.4.470

16 February 2023

1 reference

Journal of Medical Genetics

16 February 2023

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4646558%20AND%20SRC:MED&resulttype=core&format=json

1 October 2019

volume

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4646558%20AND%20SRC:MED&resulttype=core&format=json

1 October 2019

issue

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4646558%20AND%20SRC:MED&resulttype=core&format=json

1 October 2019

page(s)

470-473

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4646558%20AND%20SRC:MED&resulttype=core&format=json

Chromosome abnormalities in two cases with bilateral radial element defects

1 October 2019

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1469060

Multiple congenital malformations in a boy with a chromosome abnormality of the group F (46-XY, 20-P), the son of a clinically healthy subject with an analogous chromosome malformation

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1469060

Partial deletion of a group-F (19-20) chromosome in a physically handicapped psychiatric male patient

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1469060

[Chromosome analyses in idiopathic acquired sideroblastic anemia. A study of 6 cases]

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1469060

A SMALL AUTOSOMAL RING CHROMOSOME IN A FEMALE INFANT WITH CONGENITAL MALFORMATIONS.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1469060

Chromosomal aberrations in acute leukemia

26 October 2018

1 reference

12 December 2020

Further observations on patients with a chromosomal abnormality associated with polycythaemia vera

1 reference

12 December 2020

Partial F trisomy and parental chromosomes

1 reference

12 December 2020

Unusual Chromosomal Findings in a Case of Myelofibrosis

1 reference

12 December 2020

Analysis of human metaphase chromosome set by aid of DNA-binding fluorescent agents

1 reference

12 December 2020

Long-arm deletion of 19-20 chromosomes

1 reference

12 December 2020

Identity of the abnormal F-group chromosome associated with polycythaemia vera

1 reference

12 December 2020

Relation between Cancer and Congenital Defects in Man

5

1 reference

Mongolism and congenital leukemia

16 February 2023

8

1 reference

Congenital leukemia.Report of a case with chromosome abnormalities

16 February 2023

10

1 reference

16 February 2023

Identifiers

DOI

10.1136/JMG.9.4.470

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4646558%20AND%20SRC:MED&resulttype=core&format=json

1 October 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4646558%20AND%20SRC:MED&resulttype=core&format=json

1 October 2019

1 reference