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Carrier screening for spinal muscular atrophy
scientific article
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Statements
instance of
scholarly article
0 references
title
Carrier screening for spinal muscular atrophy
(English)
0 references
main subject
spinal muscular atrophy
1 reference
based on heuristic
inferred from title
muscular atrophy
1 reference
based on heuristic
inferred from title
author name string
Thomas W Prior
series ordinal
1
0 references
language of work or name
English
0 references
publication date
November 2008
0 references
published in
Genetics in Medicine
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volume
10
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page(s)
840-2
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issue
11
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cites work
Identification and characterization of a spinal muscular atrophy-determining gene
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3110347
retrieved
7 April 2017
Genetic testing and risk assessment for spinal muscular atrophy (SMA).
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3110347
retrieved
29 September 2017
Identification of proximal spinal muscular atrophy carriers and patients by analysis of SMNT and SMNC gene copy number
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3110347
retrieved
29 September 2017
Incidence, prevalence, and gene frequency studies of chronic childhood spinal muscular atrophy
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3110347
retrieved
29 September 2017
Molecular analysis of spinal muscular atrophy and modification of the phenotype by SMN2.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1097%2FGIM.0B013E318188D069
retrieved
21 January 2018
Prenatal prediction in families with autosomal recessive proximal spinal muscular atrophy (5q11.2-q13.3): molecular genetics and clinical experience in 109 cases
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/18941424
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1097/GIM.0B013E318188D069
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
2748589
Dimensions Publication ID
1006507920
0 references
OpenCitations bibliographic resource ID
2748589
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
2748589
PMCID
3110347
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
2748589
PubMed ID
18941424
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
2748589
Springer Nature article ID
10.1097/gim.0b013e318188d069
0 references
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