Published in
Cell Press, American Journal of Human Genetics, 3(105), p. 640-657, 2019
DOI: 10.1016/j.ajhg.2019.07.005
Links
Tools
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 
,
Berta Crespo,
Fabiola Ceroni,
Cynthia J. Curry,
Emanuele Bellacchio,
Dorine A. Bax,
Andrea Ciolfi,
Marleen Simon,
Christina R. Fagerberg ,
Ellen van Binsbergen,
Alessandro De Luca ,
Luigi Memo,
William B. Dobyns,
Alaa Afif Mohammed
and other authors.
,
Berta Crespo,
Fabiola Ceroni,
Cynthia J. Curry,
Emanuele Bellacchio,
Dorine A. Bax,
Andrea Ciolfi,
Marleen Simon,
Christina R. Fagerberg ,
Ellen van Binsbergen,
Alessandro De Luca ,
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.
Full text: Unavailable
Published version:
archiving forbidden
Data provided by 