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English
Severe hypophosphatasia due to mutations in the tissue-nonspecific alkaline phosphatase (TNSALP) gene.
scientific article
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
12416636
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12416636%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 December 2019
title
Severe hypophosphatasia due to mutations in the tissue-nonspecific alkaline phosphatase (TNSALP) gene
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
12416636
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12416636%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 December 2019
main subject
hypophosphatasia
0 references
author name string
Stoll C
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
12416636
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12416636%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 December 2019
Fischbach M
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed ID
12416636
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12416636%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 December 2019
Terzic J
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed ID
12416636
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12416636%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 December 2019
Alembik Y
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed ID
12416636
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12416636%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 December 2019
Vuillemin MO
series ordinal
5
1 reference
stated in
Europe PubMed Central
PubMed ID
12416636
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12416636%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 December 2019
Mornet E
series ordinal
6
1 reference
stated in
Europe PubMed Central
PubMed ID
12416636
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12416636%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 December 2019
publication date
1 January 2002
1 reference
stated in
Europe PubMed Central
PubMed ID
12416636
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12416636%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 December 2019
published in
Genetic Counseling
1 reference
stated in
Europe PubMed Central
PubMed ID
12416636
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12416636%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 December 2019
volume
13
1 reference
stated in
Europe PubMed Central
PubMed ID
12416636
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12416636%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 December 2019
issue
3
1 reference
stated in
Europe PubMed Central
PubMed ID
12416636
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12416636%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 December 2019
page(s)
289-295
1 reference
stated in
Europe PubMed Central
PubMed ID
12416636
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12416636%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 December 2019
Identifiers
PubMed ID
12416636
1 reference
stated in
Europe PubMed Central
PubMed ID
12416636
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12416636%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 December 2019
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