Expanding the clinical phenotype of <scp>RASopathies</scp> in 38 Turkish patients, including the rare <scp><i>LZTR1</i></scp>, <scp><i>RAF1</i></scp>, <scp><i>RIT1</i></scp> variants, and large deletion in <scp><i>NF1</i></scp>
Expanding the clinical phenotype of <scp>RASopathies</scp> in 38 Turkish patients, including the rare <scp><i>LZTR1</i></scp>, <scp><i>RAF1</i></scp>, <scp><i>RIT1</i></scp> variants, and large deletion in <scp><i>NF1</i></scp> is a paper indexed in ScholarIQ from OpenAlex.
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Expanding the clinical phenotype of <scp>RASopathies</scp> in 38 Turkish patients, including the rare <scp><i>LZTR1</i></scp>, <scp><i>RAF1</i></scp>, <scp><i>RIT1</i></scp> variants, and large deletion in <scp><i>NF1</i></scp> has 14 citations in the OpenAlex counts ScholarIQ stores.
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Expanding the clinical phenotype of <scp>RASopathies</scp> in 38 Turkish patients, including the rare <scp><i>LZTR1</i></scp>, <scp><i>RAF1</i></scp>, <scp><i>RIT1</i></scp> variants, and large deletion in <scp><i>NF1</i></scp> has 2021 year in the ScholarIQ index.
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Expanding the clinical phenotype of <scp>RASopathies</scp> in 38 Turkish patients, including the rare <scp><i>LZTR1</i></scp>, <scp><i>RAF1</i></scp>, <scp><i>RIT1</i></scp> variants, and large deletion in <scp><i>NF1</i></scp> has closed oa status in the ScholarIQ index.
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