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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Oct 4, 2023. (Total: 221739Documents)
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Records 1 - 4 (of 4 Records)

Query Trace: Learning and PTPN11[original query]
[Phenotype variability in Noonan syndrome patients with and without PTPN11 mutation].
Arquivos brasileiros de endocrinologia e metabologia 2007 Apr 51 (3): 450-6.
Ferreira Lize V, Souza Silvia A L, Montenegro Luciana R, Arnhold Ivo J P, Pasqualini Titania, Heinrich Juan Jorge, Keselman Ana Claudia, Mendonça Berenice B, Jorge Alexander A
Genotype differences in cognitive functioning in Noonan syndrome.
Genes, brain, and behavior 2009 Apr 8 (3): 275-82.
Pierpont E I, Pierpont M E, Mendelsohn N J, Roberts A E, Tworog-Dube E, Seidenberg M
Chronic pain in Noonan Syndrome: A previously unreported but common symptom.
American journal of medical genetics. Part A 2015 Aug .
Vegunta Sravanthi, Cotugno Richard, Williamson Amber, Grebe Theresa
Juvenile xanthogranuloma in Noonan syndrome.
American journal of medical genetics. Part A 2021 5 185 (10): 3048-3052.
Ali Marwan M, Gilliam Amy E, Ruben Beth S, Tidyman William E, Rauen Katherine
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