Ectrodactyly and lethal pulmonary acinar dysplasia associated with homozygous FGFR2 mutations identified by exome sequencing
Files
(Accepted version)
Date
2016
Authors
Barnett, C.
Nataren, N.
Klingler-Hoffmann, M.
Schwarz, Q.
Chong, C.
Lee, Y.
Bruno, D.
Lipsett, J.
Mcphee, A.
Schreiber, A.
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Advisors
Journal Title
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Journal article
Citation
Human Mutation, 2016; 37(9):955-963
Statement of Responsibility
Christopher P. Barnett, Nathalie J. Nataren, Manuela Klingler-Hoffmann, Quenten Schwarz, Chan-Eng Chong, Young K. Lee, Damien L. Bruno, Jill Lipsett, Andrew J. McPhee, Andreas W. Schreiber, Jinghua Feng, Christopher N. Hahn, and Hamish S. Scott
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Abstract
Abstract not available
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First published: 11 July 2016
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© 2016 Wiley Periodicals, Inc.