Use this url to cite publication: https://hdl.handle.net/20.500.12259/144470
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DCHS2, a novel autosomal recessive cause of Van Maldergem Syndrome
Type of publication
Tezės kitame recenzuojamame leidinyje / Theses in other peer-reviewed publication (T1e)
Author(s)
Voisin, Norine | Center for Integrative Genomics, University of Lausanne | CH |
Ambrozaitytė, Laima | Vilniaus universitetas | LT |
Morkūnienė, Aušra | Vilniaus universitetas | LT |
Gueneau, Lucie | Center for Integrative Genomics, University of Lausanne | CH |
Männik, Katrin | Center for Integrative Genomics, University of Lausanne | CH |
Maldžienė, Živilė | Vilniaus universitetas | LT |
Preikšaitienė, Eglė | Vilniaus universitetas | LT |
Vilniaus universitetas | LT | |
Rančelis, Tautvydas | Vilniaus universitetas | LT |
Cimbalistienė, Loreta | Vilniaus universitetas | LT |
Guex, Nicolas | Swiss Institute of Bioinformatics, Lausanne | CH |
Kučinskas, Vaidutis | Vilniaus universitetas | LT |
Reymond, Alexandre | Center for Integrative Genomics, University of Lausanne | CH |
Title
DCHS2, a novel autosomal recessive cause of Van Maldergem Syndrome
Is part of
65th Annual Meeting of The American Society of Human Genetics, October 6-10, 2015, Baltimore MD : poster abstracts. Baltimore : The American Society of Human Genetics, 2015
Date Issued
Date Issued |
---|
2015 |
Publisher
Baltimore : The American Society of Human Genetics, 2015
Extent
p. 1080
Field of Science
Type of document
type::text::conference output::conference proceedings::conference paper
Language
Anglų / English (en)
Coverage Spatial
Jungtinės Amerikos Valstijos / United States of America (US)
Other Identifier(s)
VDU02-000067747