Article Versions Notes

Taha I, De Paoli F, Foroni S, Zucca S, Limongelli I, Cipolli M, Danesino C, Ramenghi U, Minelli A. Phenotypic Variation in Two Siblings Affected with Shwachman-Diamond Syndrome: The Use of Expert Variant Interpreter (eVai) Suggests Clinical Relevance of a Variant in the KMT2A Gene. Genes. 2022; 13(8):1314. https://doi.org/10.3390/genes13081314

Taha, Ibrahim, Federica De Paoli, Selena Foroni, Susanna Zucca, Ivan Limongelli, Marco Cipolli, Cesare Danesino, Ugo Ramenghi, and Antonella Minelli. 2022. "Phenotypic Variation in Two Siblings Affected with Shwachman-Diamond Syndrome: The Use of Expert Variant Interpreter (eVai) Suggests Clinical Relevance of a Variant in the KMT2A Gene" Genes 13, no. 8: 1314. https://doi.org/10.3390/genes13081314

Taha, I., De Paoli, F., Foroni, S., Zucca, S., Limongelli, I., Cipolli, M., Danesino, C., Ramenghi, U., & Minelli, A. (2022). Phenotypic Variation in Two Siblings Affected with Shwachman-Diamond Syndrome: The Use of Expert Variant Interpreter (eVai) Suggests Clinical Relevance of a Variant in the KMT2A Gene. Genes, 13(8), 1314. https://doi.org/10.3390/genes13081314