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1 Ergebnisse
1
De Novo Missense Variants in FBXW11 Cause Diverse Developme..:
Holt, Richard J.
;
Young, Rodrigo M.
;
Crespo, Berta
...
The American Journal of Human Genetics. 105 (2019) 3 - p. 640-657 , 2019
Link:
https://doi.org/10.1016/j.ajhg.2019.07.005
RT Journal T1
De Novo Missense Variants in FBXW11 Cause Diverse Developmental Phenotypes Including Brain, Eye, and Digit Anomalies
UL https://suche.suub.uni-bremen.de/peid=cr-10.1016_j.ajhg.2019.07.005&Exemplar=1&LAN=DE A1 Holt, Richard J. A1 Young, Rodrigo M. A1 Crespo, Berta A1 Ceroni, Fabiola A1 Curry, Cynthia J. A1 Bellacchio, Emanuele A1 Bax, Dorine A. A1 Ciolfi, Andrea A1 Simon, Marleen A1 Fagerberg, Christina R. A1 van Binsbergen, Ellen A1 De Luca, Alessandro A1 Memo, Luigi A1 Dobyns, William B. A1 Mohammed, Alaa Afif A1 Clokie, Samuel J.H. A1 Zazo Seco, Celia A1 Jiang, Yong-Hui A1 Sørensen, Kristina P. A1 Andersen, Helle A1 Sullivan, Jennifer A1 Powis, Zöe A1 Chassevent, Anna A1 Smith-Hicks, Constance A1 Petrovski, Slavé A1 Antoniadi, Thalia A1 Shashi, Vandana A1 Gelb, Bruce D. A1 Wilson, Stephen W. A1 Gerrelli, Dianne PB Elsevier BV YR 2019 SN 0002-9297 JF The American Journal of Human Genetics VO 105 IS 3 SP 640 OP 657 LK http://dx.doi.org/https://doi.org/10.1016/j.ajhg.2019.07.005 DO https://doi.org/10.1016/j.ajhg.2019.07.005 SF ELIB - SuUB Bremen
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