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English
Short-limbed dwarfism: slw is a new allele of Npr2 causing chondrodysplasia.
scientific article published on 28 August 2007
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scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17728275
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17728275%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 January 2020
title
Short-limbed dwarfism: slw is a new allele of Npr2 causing chondrodysplasia
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17728275
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17728275%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 January 2020
author
Kentaro Katayama
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17728275
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17728275%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 January 2020
author name string
Chizuru Sogawa
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17728275
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17728275%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 January 2020
Takehito Tsuji
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17728275
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17728275%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 January 2020
Yusuke Shinkai
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17728275
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17728275%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 January 2020
Tetsuo Kunieda
series ordinal
5
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17728275
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17728275%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 January 2020
publication date
28 August 2007
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17728275
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17728275%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 January 2020
published in
Journal of Heredity
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17728275
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17728275%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 January 2020
volume
98
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17728275
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17728275%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 January 2020
issue
6
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17728275
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17728275%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 January 2020
page(s)
575-580
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17728275
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17728275%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 January 2020
Identifiers
DOI
10.1093/JHERED/ESM065
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17728275
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17728275%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 January 2020
PubMed publication ID
17728275
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17728275
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17728275%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 January 2020
ResearchGate publication ID
6112675
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