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Exome Sequencing Identifies WDR35 Variants Involved in Se... | ResearchHub
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Exome Sequencing Identifies WDR35 Variants Involved in Sensenbrenner Syndrome
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Authors
Christian Gilissen
13 more
Christian Gilissen
•
Dorus Mans
11 more
•
Han Brunner
Published
September 1, 2010
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Journal
The American Journal of Human Genetics
Topics
Biology
Medicine
Genetics
Molecular Biology
Mutation
Show all topics
DOI
10.1016/j.ajhg.2010.08.004
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publisher-specific-oa
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Journal
The American Journal of Human Genetics
Topics
Biology
Medicine
Genetics
Molecular Biology
Mutation
Show all topics
DOI
10.1016/j.ajhg.2010.08.004
License
publisher-specific-oa
