about
CTC1 Mutations in a patient with dyskeratosis congenita.Methylation status of the chromosome arm 19q MicroRNA cluster in sporadic and androgenetic-Biparental mosaicism-associated hepatic mesenchymal hamartoma.Monoallelic and biallelic CREB3L1 variant causes mild and severe osteogenesis imperfecta, respectively.
P50
description
investigador
@es
researcher
@en
wetenschapper
@nl
name
Rachel B Keller
@en
Rachel B Keller
@nl
type
label
Rachel B Keller
@en
Rachel B Keller
@nl
prefLabel
Rachel B Keller
@en
Rachel B Keller
@nl
P31
P496
0000-0001-6138-9257