Please use this identifier to cite or link to this item: https://observatorio.fm.usp.br/handle/OPI/58479
Title: A 43 years-old patient with Cornelia de Lange Syndrome with NIPBL gene mutation and a mild phenotype
Authors: VILELLA, ThainaNUNES, Beatriz CarvalhoPINHEIRO, IsabelAOI, HaromiMATSUMOTO, NaomichiKIM, ChongMELARAGNO, Maria Isabel
Citation: EUROPEAN JOURNAL OF HUMAN GENETICS, v.32, suppl.1, p.235-235, 2024
Appears in Collections:

Comunicações em Eventos - FM/MPE
Departamento de Pediatria - FM/MPE

Comunicações em Eventos - LIM/03
LIM/03 - Laboratório de Medicina Laboratorial

Comunicações em Eventos - LIM/36
LIM/36 - Laboratório de Pediatria Clínica


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