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English
Prenatal diagnosis of glycogen storage disease type 1a by single stranded conformation polymorphism (SSCP)
scientific article published on 01 September 1996
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8905902
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8905902%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 October 2019
title
Prenatal diagnosis of glycogen storage disease type 1a by single stranded conformation polymorphism (SSCP)
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8905902
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8905902%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 October 2019
main subject
glycogen storage disease
1 reference
based on heuristic
inferred from title
author
Eli Hershkovitz
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8905902
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8905902%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 October 2019
author name string
Parvari R
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8905902
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8905902%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 October 2019
Carmi R
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8905902
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8905902%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 October 2019
Moses S
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8905902
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8905902%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 October 2019
publication date
1 September 1996
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8905902
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8905902%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 October 2019
published in
Prenatal Diagnosis
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8905902
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8905902%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 October 2019
volume
16
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8905902
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8905902%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 October 2019
issue
9
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8905902
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8905902%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 October 2019
page(s)
862-865
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8905902
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8905902%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 October 2019
cites work
Prenatal diagnosis for cystic fibrosis using SSCP analysis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291097-0223%28199609%2916%3A9%3C862%3A%3AAID-PD954%3E3.0.CO%3B2-9
retrieved
21 January 2018
Rapid detection of medium chain acyl-CoA dehydrogenase gene mutations by non-radioactive, single strand conformation polymorphism minigels
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291097-0223%28199609%2916%3A9%3C862%3A%3AAID-PD954%3E3.0.CO%3B2-9
retrieved
21 January 2018
Point mutation screening for 16 exons of the dystrophin gene by multiplex single-strand conformation polymorphism analysis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291097-0223%28199609%2916%3A9%3C862%3A%3AAID-PD954%3E3.0.CO%3B2-9
retrieved
21 January 2018
Mutations in the glucose-6-phosphatase gene that cause glycogen storage disease type 1a
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291097-0223%28199609%2916%3A9%3C862%3A%3AAID-PD954%3E3.0.CO%3B2-9
retrieved
21 January 2018
Two founder mutations in the LDL receptor gene in Norwegian familial hypercholesterolemia subjects
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291097-0223%28199609%2916%3A9%3C862%3A%3AAID-PD954%3E3.0.CO%3B2-9
retrieved
21 January 2018
Characterization of the mutations in the glucose-6-phosphatase gene in Israeli patients with glycogen storage disease type 1a: R83C in six Jews and a novel V166G mutation in a Muslim Arab
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291097-0223%28199609%2916%3A9%3C862%3A%3AAID-PD954%3E3.0.CO%3B2-9
retrieved
21 January 2018
Molecular diagnosis of 21-hydroxylase deficiency: detection of four mutations on a single gel
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291097-0223%28199609%2916%3A9%3C862%3A%3AAID-PD954%3E3.0.CO%3B2-9
retrieved
21 January 2018
Identifiers
DOI
10.1002/(SICI)1097-0223(199609)16:9<862::AID-PD954>3.0.CO;2-9
0 references
PubMed publication ID
8905902
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8905902
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8905902%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 October 2019
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