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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2005 | 2 |
2006 | 2 |
2008 | 1 |
2012 | 1 |
2013 | 1 |
2024 | 0 |
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Diversity and functional consequences of germline and somatic PTPN11 mutations in human disease.
Am J Hum Genet. 2006 Feb;78(2):279-90. doi: 10.1086/499925. Epub 2005 Dec 7.
Am J Hum Genet. 2006.
PMID: 16358218
Free PMC article.
PTPN11 mutations play a minor role in isolated congenital heart disease.
Weismann CG, Hager A, Kaemmerer H, Maslen CL, Morris CD, Schranz D, Kreuder J, Gelb BD.
Weismann CG, et al.
Am J Med Genet A. 2005 Jul 15;136(2):146-51. doi: 10.1002/ajmg.a.30789.
Am J Med Genet A. 2005.
PMID: 15940693
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Genome wide analysis of pathogenic SH2 domain mutations.
Lappalainen I, Thusberg J, Shen B, Vihinen M.
Lappalainen I, et al.
Proteins. 2008 Aug;72(2):779-92. doi: 10.1002/prot.21970.
Proteins. 2008.
PMID: 18260110
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Atrioventricular canal defect in patients with RASopathies.
Digilio MC, Romana Lepri F, Dentici ML, Henderson A, Baban A, Roberti MC, Capolino R, Versacci P, Surace C, Angioni A, Tartaglia M, Marino B, Dallapiccola B.
Digilio MC, et al.
Eur J Hum Genet. 2013 Feb;21(2):200-4. doi: 10.1038/ejhg.2012.145. Epub 2012 Jul 11.
Eur J Hum Genet. 2013.
PMID: 22781091
Free PMC article.
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Additional evidence that PTPN11 mutations play only a minor role in the pathogenesis of non-syndromic atrioventricular canal defect.
Sarkozy A, Lepri F, Marino B, Pizzuti A, Digilio MC, Dallapiccola B.
Sarkozy A, et al.
Am J Med Genet A. 2006 Sep 15;140(18):1970-2. doi: 10.1002/ajmg.a.31394.
Am J Med Genet A. 2006.
PMID: 16892325
No abstract available.
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