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A novel PTPN11 gene mutation bridges Noonan syndrome, multiple lentigines/LEOPARD syndrome and Noonan-like/multiple giant cell lesion syndrome | European Journal of Human Genetics
CardioPekes-Cardiología Pediatrica - ‼️Conoce el Síndrome de Noonan‼️ ➡️El síndrome de #Noonan se caracteriza por: ✓Estatura baja, dismorfia facial característica y anomalías cardiacas congénitas. ✓La incidencia se estima entre 1/1.000 y 1/2.500
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Síndrome de Noonan - Grupal embrio - Síndrome de NoonaN El síndrome de Noonan es un trastorno - Studocu
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