(Q70236086)

English

Two cases of the Langer-Giedion syndrome with the same interstitial deletion of the long arm of chromosome 8: 46,XY or XX,del(8)(q23.3q24.13)

scientific article published on 01 January 1983

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6336324%20AND%20SRC:MED&resulttype=core&format=json

9 October 2019

Two cases of the Langer-Giedion syndrome with the same interstitial deletion of the long arm of chromosome 8: 46, XY or XX, del (8) (q23.3q24.13) (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6336324%20AND%20SRC:MED&resulttype=core&format=json

9 October 2019

Two cases of the Langer-Giedion syndrome with the same interstitial deletion of the long arm of chromosome 8: 46,XY or XX,del(8)(q23.3q24.13) (English)

1 reference

10.1007/BF00289486

https://api.crossref.org/works/10.1007/BF00289486

1 October 2023

chromosomal deletion syndrome

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A6336324

1 October 2023

1 reference

10.1007/BF00289486

https://api.crossref.org/works/10.1007/BF00289486

1 October 2023

author name string

Y. Fukushima

1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A6336324

1 October 2023

Y. Kuroki

2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A6336324

1 October 2023

T. Izawa

3

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A6336324

1 October 2023

language of work or name

1 reference

National Center for Biotechnology Information

PubMed publication ID

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=6336324

1 October 2023

publication date

1 January 1983

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6336324%20AND%20SRC:MED&resulttype=core&format=json

9 October 2019

full work available at URL

http://link.springer.com/content/pdf/10.1007/BF00289486.pdf

Portable Document Format

1 reference

10.1007/BF00289486

https://api.crossref.org/works/10.1007/BF00289486

1 October 2023

http://link.springer.com/article/10.1007/BF00289486/fulltext.html

1 reference

10.1007/BF00289486

https://api.crossref.org/works/10.1007/BF00289486

1 October 2023

http://link.springer.com/content/pdf/10.1007/BF00289486

1 reference

10.1007/BF00289486

https://api.crossref.org/works/10.1007/BF00289486

1 October 2023

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6336324%20AND%20SRC:MED&resulttype=core&format=json

9 October 2019

64

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6336324%20AND%20SRC:MED&resulttype=core&format=json

9 October 2019

1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6336324%20AND%20SRC:MED&resulttype=core&format=json

9 October 2019

90-93

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6336324%20AND%20SRC:MED&resulttype=core&format=json

9 October 2019

https://scigraph.springernature.com/pub.10.1007/bf00289486

0 references

Familial tricho-rhino-phalangeal syndrome Type II.

1 reference

https://pubmed.ncbi.nlm.nih.gov/6336324

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Langer-Giedion syndrome with interstitial 8q-deletion

1 reference

https://pubmed.ncbi.nlm.nih.gov/6336324

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

No chromosome deletion found on prometaphase banding in two cases of Langer-Giedion syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/6336324

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Langer-Giedion syndrome and additional congenital malformations with interstitial deletion of the long arm of chromosome 8 46, XY, del 8 (q 13-22)

1 reference

https://pubmed.ncbi.nlm.nih.gov/6336324

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An international system for human cytogenetic nomenclature--high-resolution banding (1981). ISCN (1981). Report of the Standing Committee on Human Cytogenetic Nomenclature

1 reference

https://pubmed.ncbi.nlm.nih.gov/6336324

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Langer-Giedion syndrome and deletion of the long arm of chromosome 8

1 reference

https://pubmed.ncbi.nlm.nih.gov/6336324

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

"Microcytogenetics" and Langer-Giedion syndrome.

1 reference

https://pubmed.ncbi.nlm.nih.gov/6336324

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Langer-Giedion syndrome: report of a 22-year old woman

1 reference

https://pubmed.ncbi.nlm.nih.gov/6336324

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosome deletion and multiple cartilaginous exostoses

1 reference

https://pubmed.ncbi.nlm.nih.gov/6336324

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Presumptive long arm deletion of chromosome 8: a new syndrome?

1 reference

https://pubmed.ncbi.nlm.nih.gov/6336324

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deletion of the long arm of chromosome 8 resulting from a de novo translocation t(4;8) (q13;q213)

1 reference

https://pubmed.ncbi.nlm.nih.gov/6336324

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Interstitial deletion of the long arm of chromosome 8. Karyotype: 46,XY,del(8)(q21)

1 reference

https://pubmed.ncbi.nlm.nih.gov/6336324

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Multiple exostoses-mental retardation syndrome (Ale-Calo or M.E.M.R. syndrome).

1 reference

https://pubmed.ncbi.nlm.nih.gov/6336324

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Small structural changes of chromosome 8. Two cases with evidence for deletion

1 reference

https://pubmed.ncbi.nlm.nih.gov/6336324

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00289486

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6336324%20AND%20SRC:MED&resulttype=core&format=json

9 October 2019

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6336324%20AND%20SRC:MED&resulttype=core&format=json

9 October 2019

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q70236086&oldid=1985040822"