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De novo variants in <italic>KLF7</italic> are a potential novel cause of developmental delay/intellectual disability, neuromuscular and psychiatric symptoms.
- Published in:
- Clinical Genetics, 2018, v. 93, n. 5, p. 1030, doi. 10.1111/cge.13198
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- Publication type:
- Article
Expansion and further delineation of the <italic>SETD5</italic> phenotype leading to global developmental delay, variable dysmorphic features, and reduced penetrance.
- Published in:
- Clinical Genetics, 2018, v. 93, n. 4, p. 752, doi. 10.1111/cge.13132
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- Publication type:
- Article