Evidence that the “neurofibromatosis-Noonan syndrome” is a variant of von Recklinghausen neurofibromatosis
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference8 articles.
1. Noonan phenotype associated with neurofibromatosis
2. Noonan syndrome: The changing phenotype
3. A distinctive facial appearance in neurofibromatosis von recklinghausen
4. The neurofibromatosis-Noonan syndrome
5. Noonan syndrome: A review
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1. Germline Neurofibromin 1 mutation enhances the anti‐tumour immune response and decreases juvenile myelomonocytic leukaemia tumourigenicity;British Journal of Haematology;2023-05-05
2. A Novel Heterozygous NF1 Variant in a Neurofibromatosis-Noonan Syndrome Patient with Growth Hormone Deficiency: A Case Report;Journal of Clinical Research in Pediatric Endocrinology;2022-05-31
3. Pathogenesis of Growth Failure in Rasopathies;PEDIATR ENDOCR REV P;2019
4. Neurofibromatosis-Noonan Syndrome: A Possible Paradigm of the Combination of Genetic and Epigenetic Factors;Advances in Experimental Medicine and Biology;2017
5. Growth Hormone Deficiency in a Child with Neurofibromatosis-Noonan Syndrome;Journal of Clinical Research in Pediatric Endocrinology;2016-03-01
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