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English
Male with typical fragile X phenotype is deleted for part of the FMR1 gene and for about 100 kb of upstream region.
scientific article published in July 1994
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
7943018
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7943018%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 October 2019
title
Male with typical fragile X phenotype is deleted for part of the FMR1 gene and for about 100 kb of upstream region
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
7943018
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7943018%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 October 2019
author
Yvon Trottier
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
7943018
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7943018%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 October 2019
author name string
Imbert G
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed ID
7943018
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7943018%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 October 2019
Poustka A
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed ID
7943018
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7943018%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 October 2019
Fryns JP
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed ID
7943018
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7943018%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 October 2019
Mandel JL
series ordinal
5
1 reference
stated in
Europe PubMed Central
PubMed ID
7943018
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7943018%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 October 2019
publication date
1 July 1994
1 reference
stated in
Europe PubMed Central
PubMed ID
7943018
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7943018%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 October 2019
published in
American Journal of Medical Genetics Part A
1 reference
stated in
Europe PubMed Central
PubMed ID
7943018
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7943018%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 October 2019
volume
51
1 reference
stated in
Europe PubMed Central
PubMed ID
7943018
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7943018%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 October 2019
page(s)
454-457
1 reference
stated in
Europe PubMed Central
PubMed ID
7943018
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7943018%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 October 2019
issue
4
1 reference
stated in
Europe PubMed Central
PubMed ID
7943018
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7943018%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 October 2019
Identifiers
DOI
10.1002/AJMG.1320510431
1 reference
stated in
Europe PubMed Central
PubMed ID
7943018
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7943018%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 October 2019
PubMed ID
7943018
1 reference
stated in
Europe PubMed Central
PubMed ID
7943018
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7943018%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 October 2019
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