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English
ABNORMALITIES WITH RING CHROMOSOME
scientific article published in August 1965
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
14348610
retrieved
22 April 2018
reference URL
http://europepmc.org/abstract/MED/14348610
title
ABNORMALITIES WITH RING CHROMOSOME
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
14348610
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A14348610
retrieved
20 February 2024
main subject
chromosome abnormality
1 reference
stated in
Europe PubMed Central
PubMed publication ID
14348610
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A14348610
retrieved
20 February 2024
author name string
L. E. REISMAN
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
14348610
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A14348610
retrieved
20 February 2024
A. DARNELL
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
14348610
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A14348610
retrieved
20 February 2024
J. W. MURPHY
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
14348610
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A14348610
retrieved
20 February 2024
language of work or name
English
0 references
publication date
1 August 1965
1 reference
stated in
Europe PubMed Central
PubMed publication ID
14348610
retrieved
22 April 2018
reference URL
http://europepmc.org/abstract/MED/14348610
full work available at URL
https://api.elsevier.com/content/article/PII:S0140673665908020?httpAccept=text/xml
1 reference
stated in
Crossref
DOI
10.1016/S0140-6736(65)90802-0
reference URL
https://api.crossref.org/works/10.1016/S0140-6736(65)90802-0
retrieved
20 February 2024
https://api.elsevier.com/content/article/PII:S0140673665908020?httpAccept=text/plain
1 reference
stated in
Crossref
DOI
10.1016/S0140-6736(65)90802-0
reference URL
https://api.crossref.org/works/10.1016/S0140-6736(65)90802-0
retrieved
20 February 2024
published in
The Lancet
1 reference
stated in
Europe PubMed Central
PubMed publication ID
14348610
retrieved
22 April 2018
reference URL
http://europepmc.org/abstract/MED/14348610
volume
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
14348610
retrieved
22 April 2018
reference URL
http://europepmc.org/abstract/MED/14348610
issue
7409
1 reference
stated in
Europe PubMed Central
PubMed publication ID
14348610
retrieved
22 April 2018
reference URL
http://europepmc.org/abstract/MED/14348610
page(s)
445
1 reference
stated in
Europe PubMed Central
PubMed publication ID
14348610
retrieved
22 April 2018
reference URL
http://europepmc.org/abstract/MED/14348610
cites work
Ring Chromosomes in Human Beings
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2865%2990802-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Multiple congenital abnormalities associated with ring chromosome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2865%2990802-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
THE DE LANGE SYNDROME. TYPUS AMSTELODAMENSIS.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2865%2990802-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
THE CORNELIA DE LANGE SYNDROME.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2865%2990802-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
DE LANGE SYNDROME. THE "AMSTERDAM TYPE" OF MENTAL DEFECT WITH CONGENITAL MALFORMATION.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2865%2990802-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
BRACHMAN-DE LANGE SYNDROME
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2865%2990802-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
BRACHMANN/DE LANGE SYNDROME SYNDROME.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2865%2990802-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
BRACHMANN/DE LANGE SYNDROME
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2865%2990802-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0140-6736(65)90802-0
1 reference
stated in
Europe PubMed Central
PubMed publication ID
14348610
retrieved
22 April 2018
reference URL
http://europepmc.org/abstract/MED/14348610
PubMed publication ID
14348610
1 reference
stated in
Europe PubMed Central
PubMed publication ID
14348610
retrieved
22 April 2018
reference URL
http://europepmc.org/abstract/MED/14348610
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