Hypoplastic left heart syndrome and 45X karyotype (Q33999605)

From Wikidata

Jump to navigation Jump to search

scientific article

edit

Language	Label	Description	Also known as
English	Hypoplastic left heart syndrome and 45X karyotype	scientific article

Statements

instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PubMed publication ID

3408619

retrieved

30 July 2017

title

Hypoplastic left heart syndrome and 45X karyotype (English)

1 reference

stated in

Europe PubMed Central

PubMed publication ID

3408619

retrieved

30 July 2017

main subject

karyotype

0 references

hypoplastic left heart syndrome

1 reference

based on heuristic

inferred from title

author name string

van Egmond H

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

3408619

retrieved

30 July 2017

Orye E

series ordinal

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

3408619

retrieved

30 July 2017

Praet M

series ordinal

3

1 reference

stated in

Europe PubMed Central

PubMed publication ID

3408619

retrieved

30 July 2017

Coppens M

series ordinal

4

1 reference

stated in

Europe PubMed Central

PubMed publication ID

3408619

retrieved

30 July 2017

Devloo-Blancquaert A

series ordinal

5

1 reference

stated in

Europe PubMed Central

PubMed publication ID

3408619

retrieved

30 July 2017

publication date

1 July 1988

1 reference

stated in

Europe PubMed Central

PubMed publication ID

3408619

retrieved

30 July 2017

published in

British Heart Journal

1 reference

stated in

Europe PubMed Central

PubMed publication ID

3408619

retrieved

30 July 2017

volume

60

1 reference

stated in

Europe PubMed Central

PubMed publication ID

3408619

retrieved

30 July 2017

issue

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

3408619

retrieved

30 July 2017

page(s)

69-71

1 reference

stated in

Europe PubMed Central

PubMed publication ID

3408619

retrieved

30 July 2017

cites work

Congenital anomalies associated with gonadal aplasia; review of 55 cases.

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=1216517

retrieved

5 July 2018

Anatomic and chromosomal anomalies in 639 spontaneous abortuses

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=1216517

retrieved

5 July 2018

Echocardiography reveals a high incidence of bicuspid aortic valve in Turner 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=1216517

retrieved

5 July 2018

Relation between fetal flow patterns, coarctation of the aorta, and pulmonary blood flow

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=1216517

retrieved

5 July 2018

Cardiovascular malformations in Turner's and Noonan'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=1216517

retrieved

5 July 2018

Hypoplastic left heart in a patient with 45,X/46,XX/47,XXX mosaicism

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=1216517

retrieved

5 July 2018

Characteristic cardiovascular anomalies of XO Turner syndrome, XX and XY phenotype and XO/XX Turner mosaic

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/3408619

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Retrospective and prospective epidemiological studies of 1500 karyotyped spontaneous human abortions

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/3408619

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosomal and clinical findings in 110 females with Turner syndrome

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/3408619

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

CARDIOVASCULAR MALFORMATION IN TURNER'S SYNDROME

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/3408619

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Intra-articular prednisolone 21: phosphate; a clinical trial

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/3408619

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

45/XO Turner's Syndrome in the Newborn: Report of Two Cases

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/3408619

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

PMC publication ID

1216517

1 reference

stated in

Europe PubMed Central

PubMed publication ID

3408619

retrieved

30 July 2017

PubMed publication ID

3408619

1 reference

stated in

Europe PubMed Central

PubMed publication ID

3408619

retrieved

30 July 2017

 

Sitelinks

Wikipedia(0 entries)

edit

Wikibooks(0 entries)

edit

Wikinews(0 entries)

edit

Wikiquote(0 entries)

edit

Wikisource(0 entries)

edit

Wikiversity(0 entries)

edit

Wikivoyage(0 entries)

edit

Wiktionary(0 entries)

edit

Multilingual sites(0 entries)

edit

Retrieved from "https://www.wikidata.org/w/index.php?title=Q33999605&oldid=1532099823"