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

Author:

Colley A.,Donnai D.,Evans D. G. R.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference27 articles.

1. Watson syndrome: is it a subtype of type 1 neurofibromatosis?;Allanson;J Med Genet,1991

2. Noonan phenotype associated with neurofibromatosis;Allanson;Am J Med Genet,1985

3. Gene for von Recklinghausen neurofibromatosis is in the pericentromeric region of chromosome 17;Barker;Science,1987

4. A major segment of the neurofibromatosis type 1 gene: DNA sequence, genomic structure, and point mutations;Cawthon;Cell,1990

5. Colley P. Strachan T. Hudson J. Colley A. Donnai D. Viskochil D. Wu CO Super M. Harris R. Thakker NS. Large-scale mutations at the NFl locus in patients with NFl and NFl with Noonan-syndrome-like features 1995

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