(Q33587375)

28 July 2017

title

Four new cases of ring 21 and 22 including familial transmission of ring 21 (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A839502

1 August 2022

main subject

chromosome abnormality

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A839502

1 August 2022

author name string

C. G. Palmer

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A839502

1 August 2022

M. E. Hodes

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A839502

1 August 2022

T. Reed

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A839502

1 August 2022

J. Kojetin

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A839502

1 August 2022

language of work or name

English

0 references

publication date

1 February 1977

1 reference

full work available at URL

28 July 2017

https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/839502/?tool=EBI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A839502

https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/839502/pdf/?tool=EBI

1 August 2022

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%3A839502

http://jmg.bmjjournals.com/cgi/content/abstract/14/1/54

1 August 2022

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%3A839502

https://europepmc.org/articles/PMC1013508

1 August 2022

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A839502

https://europepmc.org/articles/PMC1013508?pdf=render

1 August 2022

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%3A839502

Journal of Medical Genetics

1 August 2022

published in

1 reference

28 July 2017

volume

14

1 reference

28 July 2017

issue

1

1 reference

28 July 2017

page(s)

54-60

1 reference

On the Stabilization of a Ring Chromosome in Maize

28 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013508

Evidence for Sister-Strand Crossing over in Maize

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013508

The Production of Homozygous Deficient Tissues with Mutant Characteristics by Means of the Aberrant Mitotic Behavior of Ring-Shaped Chromosomes

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013508

A Closed X Chromosome in Drosophila Melanogaster

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013508

Comparative behavior of ring chromosomes

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013508

A 45,XX,21--child: attempt at a cytological and clinical interpretation of the karyotype

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013508

Monozygotic twins with ring chromosome 22.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013508

A "G" deletion syndrome anti-mongolism

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013508

22-ring chromosome: identification by controlled heat denaturation

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013508

21 monosomy in a retarded female infant

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013508

Ring-G chromosome, a new G-deletion syndrome?

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013508

Identification by fluorescent microscopy of the abnormal chromosomes associated with the G-deletion syndromes

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013508

An information and discriminant analysis of fingerprint patterns pertaining to identification of mongolism and mental retardation

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013508

Studies on human meiotic chromosomes from testicular tissue.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013508

Karyotype 45,XX,-21/46,XX,21q-in an infant with symptoms of G-deletion syndrome I

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013508

A case of a girl with a 21 ring chromosome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013508

Partial monosomy of a G group chromosome (45,XY,G-46,XY,Gr): report of a new case

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013508

31 October 2018

The G deletion syndromes

1 reference

12 December 2020

[Familial mosaicism with G ring]

1 reference

12 December 2020

Pairing at the chromosomal level

1 reference

12 December 2020

FAMILIAL VARIANT AUTOSOMES: NEW HUMAN CYTOGENETIC MARKERS

1 reference

12 December 2020

[Behavior of the ring chromosomes in mitosis and miosis in Antirrhinum majus L]

1 reference

12 December 2020

Points of exchange in a human no. 5 ring chromosome

1 reference

12 December 2020

A child with a 21-ring chromosome, 45XX,21minus-46,XX,21r investigated with the banding technique

1 reference

12 December 2020

Identification by fluorescence of two G rings: (46,XY,21r) G deletion syndrome I and (46, XX, 22r) G deletion syndrome II

1 reference

12 December 2020

Dermatoglyphics in the G deletion syndromes

1 reference

12 December 2020

Identification of 21 r and 22r chromosomes by quinacrine fluorescence

1 reference

12 December 2020

G-Deletion syndrome II

1 reference

12 December 2020

Double monosomy mosaicism (45,X/45,XX,21–) in a retarded child with multiple congenital malformations

1 reference

12 December 2020

Identifiers

DOI

10.1136/JMG.14.1.54

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=839502

1 August 2022

1 reference

28 July 2017

1 reference