Heterozygous missense mutations in SMARCA2 cause Nicolaides-Baraitser syndrome (original) (raw)

Phenotype and genotype in Nicolaides-Baraitser syndrome

American journal of medical genetics. Part C, Seminars in medical genetics, 2014

In-Frame Deletion and Missense Mutations of the C-Terminal Helicase Domain of SMARCA2 in Three Patients with Nicolaides-Baraitser Syndrome

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Heterozygous missense mutations in SMARCA2 cause Nicolaides-Baraitser syndrome (original) (raw)

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