No abstract available
MeSH terms
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DNA Mutational Analysis
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Exons / genetics
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Heart Defects, Congenital / genetics
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Homovanillic Acid / urine
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Humans
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Infant, Newborn
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Intracellular Signaling Peptides and Proteins
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Mutation, Missense* / genetics
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Noonan Syndrome / genetics*
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Noonan Syndrome / urine
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Protein Tyrosine Phosphatase, Non-Receptor Type 11
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Protein Tyrosine Phosphatases / genetics*
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SH2 Domain-Containing Protein Tyrosine Phosphatases
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Vanilmandelic Acid / urine
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src Homology Domains / genetics
Substances
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Intracellular Signaling Peptides and Proteins
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Vanilmandelic Acid
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PTPN11 protein, human
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Protein Tyrosine Phosphatase, Non-Receptor Type 11
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Protein Tyrosine Phosphatases
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SH2 Domain-Containing Protein Tyrosine Phosphatases
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Homovanillic Acid