Linked Life Data

15952114

Source:http://linkedlifedata.com/resource/pubmed/id/15952114

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
3
pubmed:dateCreated
2005-6-13
pubmed:abstractText
To study the clinical features and to identify homeobox D13 (HOXD13) gene mutation of the affected individuals in a Chinese synpolydactyly (SPD) kindred.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jun
pubmed:issn
1003-9406
pubmed:author
pubmed:issnType
Print
pubmed:volume
22
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
277-80
pubmed:meshHeading
pubmed:year
2005
pubmed:articleTitle
Mutation analysis of HOXD13 gene in a Chinese pedigree with synpolydactyly.
pubmed:affiliation
National Center for Birth Defects Monitoring, West China Second Hospital, Sichuan University, Chengdu, Sichuan, 610041, PR China.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't