Four new cases of ring 21 and 22 including familial transmission of ring 21 (Q33587375)

28 July 2017

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

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1 August 2022

M. E. Hodes

2

1 reference

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1 August 2022

T. Reed

3

1 reference

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1 August 2022

J. Kojetin

4

1 reference

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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

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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

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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

14

1 reference

28 July 2017

1

1 reference

28 July 2017

54-60

1 reference

On the Stabilization of a Ring Chromosome in Maize

28 July 2017

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