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Different mutations in theNF1 gene are associated with Neurofibromatosis-Noonan syndrome (NFNS)

✍ Scribed by Baralle, Diana ;Mattocks, Chris ;Kalidas, Kamini ;Elmslie, Frances ;Whittaker, Joanne ;Lees, Melissa ;Ragge, Nicola ;Patton, Michael A. ;Winter, Robin M. ;ffrench-Constant, Charles


Publisher
John Wiley and Sons
Year
2003
Tongue
English
Weight
372 KB
Volume
119A
Category
Article
ISSN
0148-7299

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## Abstract Signs of neurofibromatosis type 1 (NF1) and Noonan syndrome (NS), two distinct autosomal dominant disorders, occur together in patients reported as Watson syndrome (WS), neurofibromatosis‐Noonan syndrome (NFNS), partial LEOPARD syndrome, NS with features of NF1, and NF1 with Noonan‐like

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