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) (Q70236086)

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scientific article published on 01 January 1983

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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

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scholarly article

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Europe PubMed Central

PubMed publication ID

6336324

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

retrieved

9 October 2019

title

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

stated in

Europe PubMed Central

PubMed publication ID

6336324

reference URL

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

retrieved

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

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Crossref

DOI

10.1007/BF00289486

reference URL

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

retrieved

1 October 2023

main subject

chromosomal deletion syndrome

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6336324

reference URL

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

retrieved

1 October 2023

genetics

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Crossref

DOI

10.1007/BF00289486

reference URL

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

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1 October 2023

author name string

Y. Fukushima

series ordinal

1

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stated in

Europe PubMed Central

PubMed publication ID

6336324

reference URL

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

retrieved

1 October 2023

Y. Kuroki

series ordinal

2

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stated in

Europe PubMed Central

PubMed publication ID

6336324

reference URL

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

retrieved

1 October 2023

T. Izawa

series ordinal

3

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6336324

reference URL

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

retrieved

1 October 2023

language of work or name

English

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National Center for Biotechnology Information

PubMed publication ID

6336324

reference URL

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

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1 October 2023

publication date

1 January 1983

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Europe PubMed Central

PubMed publication ID

6336324

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

retrieved

9 October 2019

full work available at URL

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

file format

Portable Document Format

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Crossref

DOI

10.1007/BF00289486

reference URL

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

retrieved

1 October 2023

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

file format

HTML

1 reference

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Crossref

DOI

10.1007/BF00289486

reference URL

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

retrieved

1 October 2023

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

1 reference

stated in

Crossref

DOI

10.1007/BF00289486

reference URL

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

retrieved

1 October 2023

published in

Human Genetics

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6336324

reference URL

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

retrieved

9 October 2019

volume

64

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6336324

reference URL

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

retrieved

9 October 2019

issue

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6336324

reference URL

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

retrieved

9 October 2019

page(s)

90-93

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stated in

Europe PubMed Central

PubMed publication ID

6336324

reference URL

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

retrieved

9 October 2019

cites work

Familial tricho-rhino-phalangeal syndrome Type II.

1 reference

stated in

PubMed

reference URL

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

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Langer-Giedion syndrome with interstitial 8q-deletion

1 reference

stated in

PubMed

reference URL

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

retrieved

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

stated in

PubMed

reference URL

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

retrieved

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

stated in

PubMed

reference URL

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

retrieved

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

stated in

PubMed

reference URL

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

retrieved

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

stated in

PubMed

reference URL

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

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

"Microcytogenetics" and Langer-Giedion syndrome.

1 reference

stated in

PubMed

reference URL

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

retrieved

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

stated in

PubMed

reference URL

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

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosome deletion and multiple cartilaginous exostoses

1 reference

stated in

PubMed

reference URL

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

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

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

retrieved

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

stated in

PubMed

reference URL

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

retrieved

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

stated in

PubMed

reference URL

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

retrieved

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

stated in

PubMed

reference URL

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

retrieved

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

stated in

PubMed

reference URL

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

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1007/BF00289486

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6336324

reference URL

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

retrieved

9 October 2019

PubMed publication ID

6336324

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6336324

reference URL

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

retrieved

9 October 2019

 

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