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Foroni, Selena
7
results:
Search for persons
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Online (7)
Mediatypes
Articles (Online) (3)
OpenAccess-fulltext (4)
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1
The pathogenic variant c.258+533_459+403del in SBDS gene is..:
Foroni, Selena
;
Taha, Ibrahim
;
Bezzerri, Valentino
...
Gene Reports. 31 (2023) - p. 101775 , 2023
Link:
https://doi.org/10.1016/..
?
2
Case Report: Heterozygous Germline Variant in EIF6 Addition..:
Taha, Ibrahim
;
Foroni, Selena
;
Valli, Roberto
...
Frontiers in Genetics. 13 (2022) - p. , 2022
Link:
https://doi.org/10.3389/..
?
3
Phenotypic Variation in Two Siblings Affected with Shwachma..:
Taha, Ibrahim
;
De Paoli, Federica
;
Foroni, Selena
...
Genes. 13 (2022) 8 - p. 1314 , 2022
Link:
https://doi.org/10.3390/..
?
4
Phenotypic Variation in Two Siblings Affected with Shwachma..:
Taha, Ibrahim
;
De Paoli, Federica
;
Foroni, Selena
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9394309/. , 2022
Link:
http://www.ncbi.nlm.nih...
?
5
Phenotypic Variation in Two Siblings Affected with Shwachma..:
Ibrahim Taha
;
Federica De Paoli
;
Selena Foroni
...
Human Genomics and Genetic Diseases. , 2022
Link:
https://doi.org/10.3390/..
?
6
Phenotypic Variation in Two Siblings Affected with Shwachma..:
Ibrahim Taha
;
Federica De Paoli
;
Selena Foroni
...
https://www.mdpi.com/2073-4425/13/8/1314. , 2022
Link:
https://doi.org/10.3390/..
?
7
Case Report: Heterozygous Germline Variant in EIF6 Addition..:
Ibrahim Taha
;
Selena Foroni
;
Roberto Valli
...
https://www.frontiersin.org/articles/10.3389/fgene.2022.896749/full. , 2022
Link:
https://doi.org/10.3389/..
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