Concepedia

Publication | Open Access

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

DOIFull Paper Access

57

Citations

66

References

2019

Year

Richard Holt, Rodrigo Young, Berta Crespo, Fabiola Ceroni, Cynthia J. Curry, Emanuele Bellacchio, Dorine A. Bax, Andrea Ciolfi, Marleen Simon, Christina Fagerberg,
The American Journal of Human Genetics

References

YearCitations

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