Paternal Germline Origin and Sex-Ratio Distortion in Transmission of PTPN11 Mutations in Noonan Syndrome
Author:
Publisher
Elsevier BV
Subject
Genetics (clinical),Genetics
Reference45 articles.
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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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