Different mutations in theNF1 gene are associated with Neurofibromatosis-Noonan syndrome (NFNS)-Reference-Cited by-同舟云学术

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

Published:2003-04-16 Issue:1 Volume:119A Page:1-8
ISSN:0148-7299
Container-title:American Journal of Medical Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

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

Publisher

Wiley

Subject

Genetics (clinical)

Reference20 articles.

1. Noonan phenotype associated with neurofibromatosis

2. Novel recurrent nonsense mutation causing neurofibromatosis type 1 (NF1) in a family segregating both NF1 and Noonan syndrome

3. Neurofibromatosis/Noonan phenotype: a variable feature of type 1 neurofibromatosis

4. Mechanism for the learning deficits in a mouse model of neurofibromatosis type 1

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