about
Next-generation-based targeted sequencing as an efficient tool for the study of the genetic background in Hirschsprung patientsIdentification of epistatic interactions through genome-wide association studies in sporadic medullary and juvenile papillary thyroid carcinomas.Unravelling the genetic basis of simplex Retinitis Pigmentosa cases.Searching the second hit in patients with inherited retinal dystrophies and monoallelic variants in ABCA4, USH2A and CEP290 by whole-gene targeted sequencing
P50
description
hulumtuese
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Marta Martín-Sánchez
@ast
Marta Martín-Sánchez
@en
Marta Martín-Sánchez
@es
Marta Martín-Sánchez
@nl
type
label
Marta Martín-Sánchez
@ast
Marta Martín-Sánchez
@en
Marta Martín-Sánchez
@es
Marta Martín-Sánchez
@nl
prefLabel
Marta Martín-Sánchez
@ast
Marta Martín-Sánchez
@en
Marta Martín-Sánchez
@es
Marta Martín-Sánchez
@nl
P106
P21
P31
P496
0000-0002-1355-8834