Overlapping phenotypes between SHORT and Noonan syndromes in patients with PTPN11 pathogenic variants.
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PMID: 32233106 [PubMed - as supplied by publisher]
Source: Clinical Genetics - Category: Genetics & Stem Cells Authors: Ranza E, Guimier A, Verloes A, Capri Y, Marques C, Auclair M, Mathieu-Dramard M, Morin G, Thevenon J, Faivre L, Thauvin-Robinet C, Innes AM, Dyment DA, Vigouroux C, Amiel J Tags: Clin Genet Source Type: research