De Novo Missense Variants in FBXW11 Cause Diverse Developmental Phenotypes Including Brain, Eye, and Digit Anomalies
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Published in | American journal of human genetics Vol. 105; no. 3; pp. 640 - 657 |
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Main Authors | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
05.09.2019
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Online Access | Get full text |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
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ISSN: | 0002-9297 1537-6605 |
DOI: | 10.1016/j.ajhg.2019.07.005 |