(Q53889318)

English

Morphologic abnormality due to duplication of chromosome 17 (46,XY,17q+) in a newborn infant

scientific article published on August 1, 1974

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Europe PubMed Central

PubMed publication ID

4849205

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4849205%20AND%20SRC:MED&resulttype=core&format=json

retrieved

5 October 2019

title

Morphologic abnormality due to duplication of chromosome 17 (46,XY,17q+) in a newborn infant (English)

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marking inconsistent with the registered/official identifier/name

1 reference

stated in

Europe PubMed Central

PubMed publication ID

4849205

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A4849205

retrieved

11 March 2023

main subject

human chromosomes 16-18

1 reference

stated in

Europe PubMed Central

PubMed publication ID

4849205

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A4849205

retrieved

11 March 2023

trisomy

1 reference

stated in

Europe PubMed Central

PubMed publication ID

4849205

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A4849205

retrieved

11 March 2023

author name string

B. Fouquette

series ordinal

1

1 reference

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Europe PubMed Central

PubMed publication ID

4849205

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A4849205

retrieved

11 March 2023

R. Rosenfeld

series ordinal

2

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stated in

Europe PubMed Central

PubMed publication ID

4849205

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A4849205

retrieved

11 March 2023

M. Cadotte

series ordinal

3

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stated in

Europe PubMed Central

PubMed publication ID

4849205

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A4849205

retrieved

11 March 2023

language of work or name

French

1 reference

stated in

National Center for Biotechnology Information

PubMed publication ID

4849205

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=4849205

retrieved

11 March 2023

publication date

1 August 1974

1 reference

stated in

Europe PubMed Central

PubMed publication ID

4849205

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4849205%20AND%20SRC:MED&resulttype=core&format=json

retrieved

5 October 2019

published in

L’Union médicale du Canada

1 reference

stated in

Europe PubMed Central

PubMed publication ID

4849205

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4849205%20AND%20SRC:MED&resulttype=core&format=json

retrieved

5 October 2019

volume

103

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stated in

Europe PubMed Central

PubMed publication ID

4849205

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4849205%20AND%20SRC:MED&resulttype=core&format=json

retrieved

5 October 2019

issue

8

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Europe PubMed Central

PubMed publication ID

4849205

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4849205%20AND%20SRC:MED&resulttype=core&format=json

retrieved

5 October 2019

page(s)

1404-1408

1 reference

stated in

Europe PubMed Central

PubMed publication ID

4849205

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4849205%20AND%20SRC:MED&resulttype=core&format=json

retrieved

5 October 2019

Identifiers

PubMed publication ID

4849205

1 reference

stated in

Europe PubMed Central

PubMed publication ID

4849205

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4849205%20AND%20SRC:MED&resulttype=core&format=json

(Q53889318)

Morphologic abnormality due to duplication of chromosome 17 (46,XY,17q+) in a newborn infant

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