Somatic stigmata of Turner's syndrome in a patient with 46,XXq- (Q34635014)

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scientific article published on September 1, 1971

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Language	Label	Description	Also known as
English	Somatic stigmata of Turner's syndrome in a patient with 46,XXq-	scientific article published on September 1, 1971

Statements

instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PMC publication ID

1469177

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5097143%20AND%20SRC:MED&resulttype=core&format=json

retrieved

12 October 2019

title

Somatic stigmata of Turner's syndrome in a patient with 46,XXq- (English)

1 reference

stated in

Europe PubMed Central

PMC publication ID

1469177

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5097143%20AND%20SRC:MED&resulttype=core&format=json

retrieved

12 October 2019

main subject

sex chromosome aberration

1 reference

stated in

Europe PubMed Central

PubMed publication ID

5097143

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5097143

retrieved

16 April 2023

genetics

1 reference

stated in

Crossref

DOI

10.1136/JMG.8.3.358

reference URL

https://api.crossref.org/works/10.1136/JMG.8.3.358

retrieved

16 April 2023

author name string

M. Bocian

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

5097143

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5097143

retrieved

16 April 2023

E. Krmpotic

series ordinal

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

5097143

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5097143

retrieved

16 April 2023

K. Szego

series ordinal

3

1 reference

stated in

Europe PubMed Central

PubMed publication ID

5097143

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5097143

retrieved

16 April 2023

I. M. Rosenthal

series ordinal

4

1 reference

stated in

Europe PubMed Central

PubMed publication ID

5097143

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5097143

retrieved

16 April 2023

language of work or name

English

0 references

publication date

1 September 1971

1 reference

stated in

Europe PubMed Central

PMC publication ID

1469177

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5097143%20AND%20SRC:MED&resulttype=core&format=json

retrieved

12 October 2019

full work available at URL

https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/5097143/pdf/?tool=EBI

file format

Portable Document Format

online access status

open access

1 reference

stated in

Europe PubMed Central

PubMed publication ID

5097143

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5097143

retrieved

16 April 2023

https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/5097143/?tool=EBI

file format

HTML

online access status

open access

1 reference

stated in

Europe PubMed Central

PubMed publication ID

5097143

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5097143

retrieved

16 April 2023

https://europepmc.org/articles/PMC1469177

file format

HTML

online access status

open access

content deliverer

Europe PubMed Central

1 reference

stated in

Europe PubMed Central

PubMed publication ID

5097143

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5097143

retrieved

16 April 2023

https://europepmc.org/articles/PMC1469177?pdf=render

file format

Portable Document Format

online access status

open access

content deliverer

Europe PubMed Central

1 reference

stated in

Europe PubMed Central

PubMed publication ID

5097143

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5097143

retrieved

16 April 2023

https://syndication.highwire.org/content/doi/10.1136/jmg.8.3.358

1 reference

stated in

Crossref

DOI

10.1136/JMG.8.3.358

reference URL

https://api.crossref.org/works/10.1136/JMG.8.3.358

retrieved

16 April 2023

https://jmg.bmj.com/content/jmedgenet/8/3/358.full.pdf

file format

Portable Document Format

online access status

open access

1 reference

stated in

Europe PubMed Central

PubMed publication ID

5097143

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5097143

retrieved

15 December 2023

published in

Journal of Medical Genetics

1 reference

stated in

Europe PubMed Central

PMC publication ID

1469177

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5097143%20AND%20SRC:MED&resulttype=core&format=json

retrieved

12 October 2019

volume

8

1 reference

stated in

Europe PubMed Central

PMC publication ID

1469177

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5097143%20AND%20SRC:MED&resulttype=core&format=json

retrieved

12 October 2019

issue

3

1 reference

stated in

Europe PubMed Central

PMC publication ID

1469177

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5097143%20AND%20SRC:MED&resulttype=core&format=json

retrieved

12 October 2019

page(s)

358-363

1 reference

stated in

Europe PubMed Central

PMC publication ID

1469177

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5097143%20AND%20SRC:MED&resulttype=core&format=json

retrieved

12 October 2019

cites work

KARYOTYPE-PHENOTYPE CORRELATIONS IN GONADAL DYSGENESIS AND THEIR BEARING ON THE PATHOGENESIS OF MALFORMATIONS

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1469177

retrieved

7 July 2018

H3-THYMIDINE UPTAKE BY A RING X CHROMOSOME IN A HUMAN FEMALE

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1469177

retrieved

7 July 2018

Chromosome preparations of leukocytes cultured from human peripheral blood

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1469177

retrieved

7 July 2018

Apparent deletion of X chromosome in a prepuberal girl

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1469177

retrieved

7 July 2018

A family with D-D translocation

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1469177

retrieved

7 July 2018

Xq- Turner's syndrome: reconsideration of hypothesis that Xp- causes somatic features in Turner's syndrome

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1469177

retrieved

7 July 2018

Personality and intelligence in Turner's syndrome. A critical review

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1469177

retrieved

7 July 2018

Chromosomes and abortions

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1469177

retrieved

7 July 2018

Cytogenetic studies in primary amenorrhoea

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/5097143

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The pattern of X-chromosome deoxy-ribonucleic acid synthesis in two women with abnormal sex-chromosome complements

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/5097143

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

DERMATOGLYPHIC ANOMALIES IN TURNER'S SYNDROME

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/5097143

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

OVARIAN DYSGENESIS DUE TO DELETION OF THE X CHROMOSOME

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/5097143

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

On a case of XXdc ovarian dysgenesis

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/5097143

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Identification of the Chromosomes of the E Group (16–18 Denver): An Autoradiographic and Measurement Study

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/5097143

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Two cases of primary amenorrhea with deletion of the long arm of the X chromosome (46, XXq−)

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/5097143

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Spontaneous abortion. Chromosome studies on 41 cases and an analysis of maternal age and duration of pregnancy in relation to karyotype

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/5097143

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gonadal dysgenesis with lymphocytic thyroiditis and deletion of the long arm of the X chromosome

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/5097143

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic and clinical considerations of long-arm deletion of the X chromosome

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/5097143

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cytogenetic studies in primary amenorrhea

series ordinal

14

1 reference

stated in

Crossref

DOI

10.1136/JMG.8.3.358

reference URL

https://api.crossref.org/works/10.1136/JMG.8.3.358

retrieved

16 April 2023

Identifiers

DOI

10.1136/JMG.8.3.358

1 reference

stated in

Europe PubMed Central

PMC publication ID

1469177

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5097143%20AND%20SRC:MED&resulttype=core&format=json

retrieved

12 October 2019

PMC publication ID

1469177

1 reference

stated in

Europe PubMed Central

PMC publication ID

1469177

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5097143%20AND%20SRC:MED&resulttype=core&format=json

retrieved

12 October 2019

PubMed publication ID

5097143

1 reference

stated in

Europe PubMed Central

PMC publication ID

1469177

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5097143%20AND%20SRC:MED&resulttype=core&format=json

retrieved

12 October 2019

 

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