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KAT6A Syndrome
KAT6A Syndrome: genotype-phenotype correlation in 76 patients with pathogenic KAT6A variants
De Novo and Inherited Loss-of-Function Variants in TLK2: Clinical and Genotype-Phenotype Evaluation of a Distinct Neurodevelopmental Disorder
Experiences and Lessons from a Multicountry NIDIAG Study on Persistent Digestive Disorders in the Tropics
Diagnosis of neglected tropical diseases among patients with persistent digestive disorders (diarrhoea and/or abdominal pain >= 14 days): a multi-country, prospective, non-experimental case-control study (vol 15, 338, 2015)