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De novo mutations in PLXND1 and REV3L cause Möbius syndromeIn silico identification of new candidate genes for hereditary congenital facial paresis.Exome sequencing of Pakistani consanguineous families identifies 30 novel candidate genes for recessive intellectual disability.Crypto-rhombomeres of the mouse medulla oblongata, defined by molecular and morphological features.Variants affecting diverse domains of MEPE are associated with two distinct bone disorders, a craniofacial bone defect and otosclerosisCorrection: Exome sequencing of Pakistani consanguineous families identifies 30 novel candidate genes for recessive intellectual disability
P50
description
investigador
@es
researcher
@en
wetenschapper
@nl
name
Laura Tomás-Roca
@en
Laura Tomás-Roca
@nl
type
label
Laura Tomás-Roca
@en
Laura Tomás-Roca
@nl
prefLabel
Laura Tomás-Roca
@en
Laura Tomás-Roca
@nl
P31
P496
0000-0003-0851-0833