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Genotype differences in cognitive functioning in Noonan syndrome
Noonan syndrome (NS) is an autosomal dominant genetic disorder associated with highly variable features, including heart disease, short stature, minor facial anomalies and learning disabilities. Recent gene discoveries have laid the groundwork for exploring whether variability in the NS phenotype is...
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| Hlavní autoři: | , , , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
2008
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2760992/ https://ncbi.nlm.nih.gov/pubmed/19077116 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1601-183X.2008.00469.x |
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