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Cell Press, American Journal of Human Genetics, 3(105), p. 640-657, 2019

DOI: 10.1016/j.ajhg.2019.07.005

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De Novo Missense Variants in FBXW11 Cause Diverse Developmental Phenotypes Including Brain, Eye, and Digit Anomalies

Journal article published in 2019 by Richard J. Holt, Rodrigo M. Young ORCID, Berta Crespo, Fabiola Ceroni, Cynthia J. Curry, Emanuele Bellacchio, Dorine A. Bax, Andrea Ciolfi, Marleen Simon, Christina R. Fagerberg ORCID, Ellen van Binsbergen, Alessandro De Luca ORCID, Luigi Memo, William B. Dobyns, Alaa Afif Mohammed and other authors.
This paper was not found in any repository, but could be made available legally by the author.
This paper was not found in any repository, but could be made available legally by the author.

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