Paternal Germline Origin and Sex-Ratio Distortion in Transmission of PTPN11 Mutations in Noonan Syndrome

Author:

Tartaglia Marco,Cordeddu Viviana,Chang Hong,Shaw Adam,Kalidas Kamini,Crosby Andrew,Patton Michael A.,Sorcini Mariella,van der Burgt Ineke,Jeffery Steve,Gelb Bruce D.

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference45 articles.

1. Noonan syndrome;Allanson;J Med Genet,1987

2. A recurrent mutation in the tyrosine kinase domain of fibroblast growth factor receptor 3 causes hypochondroplasia;Bellus;Nat Genet,1995

3. Unexpectedly similar rates of nucleotide substitution found in male and female hominids;Bohossian;Nature,2000

4. Parent-of-origin effects in multiple endocrine neoplasia type 2B;Carlson;Am J Hum Genet,1994

5. Grouping of multiple-lentigines/LEOPARD and Noonan syndromes on the PTPN11 gene;Digilio;Am J Hum Genet,2002

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