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Cardiofaciocutaneous syndrome 1
- Noonan Syndrome (For Parents) (Nemours Foundation)... loss, gene mutation, bleeding disorders, syndrome, syndromes, RASopathies, cardiofaciocutaneous syndrome, Costello syndrome, neurofibromatosis type 1, Legius syndrome, Noonan syndrome with multiple lentigines, familial ...
- Neurofibromatosis Type 1 (For Parents) (Nemours Foundation)Neurofibromatosis type 1, neurofibromatosis, nf, nf1, nf2, nfI, nfII, neurofibromas, genetic disorders, genetic testing, nerves, tumors, macrocephaly, ...
