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The p.Gly130Val mutation in the GJB2 gene: A familiar case of autosomal dominant non-syndromic hearing loss.
Int J Pediatr Otorhinolaryngol. 2019 Dec;127:109653. doi: 10.1016/j.ijporl.2019.109653. Epub 2019 Aug 22.
Int J Pediatr Otorhinolaryngol. 2019.
PMID: 31472357
A new acute myeloid leukemia case with STAT5B-RARA gene fusion due to 17q21.2 interstitial deletion.
Pessina C, Basilico C, Genoni A, Meroni E, Elli L, Granata P, Righi R, Pallotti F, Mora B, Ferrario A, Passamonti F, Casalone R.
Pessina C, et al. Among authors: meroni e.
Leuk Lymphoma. 2017 Aug;58(8):1977-1980. doi: 10.1080/10428194.2016.1262952. Epub 2016 Dec 2.
Leuk Lymphoma. 2017.
PMID: 27911132
No abstract available.
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