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Foroni, Selena
7  Ergebnisse:
Personensuche X
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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/..
 
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2

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/..
 
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3

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/..
 
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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...
 
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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/..
 
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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/..
 
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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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