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Síndrome de Noonan - Grupal embrio - Síndrome de NoonaN El síndrome de Noonan es un trastorno - Studocu
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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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
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Overlapping phenotypes between SHORT and Noonan syndromes in patients with PTPN11 pathogenic variants - Ranza - 2020 - Clinical Genetics - Wiley Online Library
![Le syndrome de Noonan n'est pas rare. Comment le reconnaître? Comment prendre en charge les patients? - pédiatrie suisse Le syndrome de Noonan n'est pas rare. Comment le reconnaître? Comment prendre en charge les patients? - pédiatrie suisse](https://cdn.paediatrieschweiz.ch/production/uploads/2021/09/Abb-2-modifie.png)
Le syndrome de Noonan n'est pas rare. Comment le reconnaître? Comment prendre en charge les patients? - pédiatrie suisse
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