Publicações

Upf3B Gene Deletion in a Patient with Severe Intellectual Disability, Epilepsy, Absent Speech: Problematic of Array-Cgh Coverage

AuthID
P-00R-5XS

Author(s)

Melo, JB

Ferreira, SI

Ramos, L

Pinto, M

Jardim, A

Carreira, IM

Tipo de Documento

Abstract

Year published

2019

Publicado

in EUROPEAN JOURNAL OF HUMAN GENETICS, ISSN: 1018-4813

Volume: 27, Páginas: 943-943 (1)

Conference

51St Conference of the European-Society-Of-Human-Genetics (Eshg) in Conjunction with the European Meeting on Psychosocial Aspects of Genetics (Empag), Date: JUN 16-19, 2018, Location: Milan, ITALY, Patrocinadores: European Soc Human Genet

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