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Homozygous WNT10b mutation and complex inheritance in Split-Hand/Foot Malformation
scientific article
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
18515319
retrieved
4 August 2017
title
Homozygous WNT10b mutation and complex inheritance in Split-Hand/Foot Malformation
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
18515319
retrieved
4 August 2017
main subject
homozygosity
1 reference
based on heuristic
inferred from title
author
Sibel Aylin Ugur
object named as
Sibel Aylin Ugur
series ordinal
1
0 references
author name string
Aslihan Tolun
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed ID
18515319
retrieved
4 August 2017
language of work or name
English
1 reference
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inferred from title
publication date
30 May 2008
1 reference
stated in
Europe PubMed Central
PubMed ID
18515319
retrieved
4 August 2017
published in
Human Molecular Genetics
1 reference
stated in
Europe PubMed Central
PubMed ID
18515319
retrieved
4 August 2017
volume
17
1 reference
stated in
Europe PubMed Central
PubMed ID
18515319
retrieved
4 August 2017
page(s)
2644-2653
1 reference
stated in
Europe PubMed Central
PubMed ID
18515319
retrieved
4 August 2017
issue
17
1 reference
stated in
Europe PubMed Central
PubMed ID
18515319
retrieved
4 August 2017
Identifiers
DOI
10.1093/HMG/DDN164
1 reference
stated in
Europe PubMed Central
PubMed ID
18515319
retrieved
4 August 2017
Fatcat ID
release_kbelnveptvhkfofmc56abkbp7u
1 reference
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Fatcat
reference URL
https://api.fatcat.wiki/v0/release/kbelnveptvhkfofmc56abkbp7u
retrieved
24 November 2022
based on heuristic
mapped directly with Wikidata item
PubMed ID
18515319
1 reference
stated in
Europe PubMed Central
PubMed ID
18515319
retrieved
4 August 2017
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