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Uma forma rara de linfoma não-Hodgkin maligno de células B maduras.
Nenhum ensaio clínico registrado para esta condição.
Addressing psychosocial vulnerability in rare diseases: a call to action from a European expert consensus study.
Machine learning-augmented biomarkers in mid-pregnancy Down syndrome screening improve prediction of small-for-gestational-age infants.
Cronkhite‒Canada syndrome as inflammatory hamartomatous polyposis: new evidence from whole transcriptome sequencing of colonic polyps.
Correction to: Diagnostic utility of next-generation sequencing-based panel testing in 543 patients with suspected skeletal dysplasia.
Diagnostic utility of next-generation sequencing-based panel testing in 543 patients with suspected skeletal dysplasia.